STRIDE-DB

Repeat Length	AFR	AMR	EUR	EAS	SAS	Repeat
25.0	2	0	0	4	6	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGATGCTGCTGCTGCTGCTGCTGCTGCT
27.0	6	0	2	12	6	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGATGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT
30.0	0	0	0	0	0	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGATGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT
22.0	2	0	0	2	4	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGATGCTGCTGCTGCTGCT
23.0	0	2	0	2	2	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGATGCTGCTGCTGCTGCTGCT
24.0	0	0	2	2	0	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGATGCTGCTGCTGCTGCTGCTGCT
26.0	3	0	0	2	6	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGATGCTGCTGCTGCTGCTGCTGCTGCTGCT
28.0	6	2	2	2	4	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGATGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT
29.0	0	4	0	0	0	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGATGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT
14.0	0	0	0	0	2	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT
15.0	1	0	0	0	4	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGAT
16.0	2	0	0	0	0	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCT
17.0	1	0	0	2	0	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGAT
18.0	0	0	0	0	2	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGATGCT
19.0	8	1	0	2	2	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGATGCTGCT
20.0	31	0	0	0	0	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGATGCTGCTGCT
21.0	18	3	0	0	2	GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGATGCTGATGCTGCTGCTGCT

Position	Disease/Trait	P-value	SNPs	Location with respect to STR	distance	Study
6:16281187	Red blood cell count,	2.0E-17	rs6914805	downstream	-46679	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
6:16281187	Mean corpuscular hemoglobin,	1.0E-18	rs6914805	downstream	-46679	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16281187	Mean corpuscular volume,	4.0E-70	rs6914805	downstream	-46679	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16281187	Mean spheric corpuscular volume,	2.0E-9	rs6914805	downstream	-46679	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16282519	High light scatter reticulocyte percentage of red cells,	3.0E-15	rs869167739	downstream	-45347	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16282519	High light scatter reticulocyte count,	1.0E-12	rs869167739	downstream	-45347	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16282519	Mean corpuscular volume,	4.0E-43	rs869167739	downstream	-45347	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16282519	Reticulocyte fraction of red cells,	6.0E-16	rs869167739	downstream	-45347	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16282519	Reticulocyte count,	3.0E-11	rs869167739	downstream	-45347	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16282519	High light scatter reticulocyte count,	1.0E-28	rs11298204	downstream	-45347	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16282519	High light scatter reticulocyte percentage of red cells,	2.0E-35	rs11298204	downstream	-45347	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16282519	Red blood cell count,	2.0E-15	rs11298204	downstream	-45347	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16282519	Reticulocyte count,	3.0E-29	rs11298204	downstream	-45347	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16282519	Reticulocyte fraction of red cells,	3.0E-39	rs11298204	downstream	-45347	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16286061	Reticulocyte fraction of red cells,	1.0E-10	rs146771786	downstream	-41805	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16286061	Reticulocyte count,	4.0E-9	rs146771786	downstream	-41805	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16286061	High light scatter reticulocyte count,	2.0E-31	rs146771786	downstream	-41805	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16286061	Mean corpuscular hemoglobin concentration,	6.0E-54	rs146771786	downstream	-41805	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
6:16286061	Mean corpuscular volume,	7.0E-43	rs146771786	downstream	-41805	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
6:16286061	Red cell distribution width,	5.0E-15	rs146771786	downstream	-41805	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
6:16286061	Reticulocyte count,	9.0E-33	rs146771786	downstream	-41805	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
6:16286061	High light scatter reticulocyte count,	3.0E-31	rs146771786	downstream	-41805	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
6:16286061	Mean corpuscular hemoglobin,	2.0E-12	rs146771786	downstream	-41805	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16286061	High light scatter reticulocyte percentage of red cells,	1.0E-35	rs146771786	downstream	-41805	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16286061	Immature fraction of reticulocytes,	1.0E-10	rs146771786	downstream	-41805	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16286061	Red cell distribution width,	1.0E-14	rs146771786	downstream	-41805	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16286061	Reticulocyte count,	1.0E-33	rs146771786	downstream	-41805	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16286061	Reticulocyte fraction of red cells,	1.0E-40	rs146771786	downstream	-41805	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16286061	Mean corpuscular hemoglobin concentration,	1.0E-19	rs146771786	downstream	-41805	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16286061	Mean corpuscular hemoglobin,	4.0E-53	rs146771786	downstream	-41805	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16286061	Mean corpuscular volume,	4.0E-36	rs146771786	downstream	-41805	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16288192	Hemoglobin levels,	8.0E-21	rs6459467	downstream	-39674	Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis.
6:16288192	Hemoglobin concentration,	3.0E-10	rs6459467	downstream	-39674	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16288192	Mean corpuscular hemoglobin concentration,	4.0E-27	rs6459467	downstream	-39674	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16288192	Blood metabolite levels,	2.0E-16	rs6459467	downstream	-39674	An atlas of genetic influences on human blood metabolites.
6:16288192	Mean corpuscular hemoglobin,	2.0E-59	rs6459467	downstream	-39674	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16288615	Red cell distribution width,	2.0E-18	rs2327958	downstream	-39251	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
6:16288615	Hemoglobin concentration,	2.0E-27	rs2327958	downstream	-39251	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
6:16288615	Mean corpuscular volume,	6.0E-142	rs2327958	downstream	-39251	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
6:16289909	Hemoglobin,	1.0E-20	rs71535075	downstream	-37957	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16289912	Hemoglobin,	9.0E-20	rs397758183	downstream	-37954	A cross-population atlas of genetic associations for 220 human phenotypes.
6:16289912	Mean corpuscular hemoglobin concentration,	5.0E-41	rs397758183	downstream	-37954	A cross-population atlas of genetic associations for 220 human phenotypes.
6:16290761	QT interval,	3.0E-6	rs1042391	downstream	-37105	ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals.
6:16290761	Mean corpuscular hemoglobin concentration,	2.0E-70	rs1042391	downstream	-37105	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
6:16290761	Hemoglobin concentration,	2.0E-28	rs1042391	downstream	-37105	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
6:16290761	Mean corpuscular hemoglobin concentration,	4.0E-76	rs1042391	downstream	-37105	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
6:16290761	Mean corpuscular volume,	1.0E-65	rs1042391	downstream	-37105	Assessing the impact of alcohol consumption on the genetic contribution to mean corpuscular volume.
6:16290761	Mean corpuscular hemoglobin concentration,	2.0E-13	rs1042391	downstream	-37105	A cross-population atlas of genetic associations for 220 human phenotypes.
6:16290761	Mean corpuscular hemoglobin concentration,	3.0E-56	rs1042391	downstream	-37105	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16290849	High light scatter reticulocyte count,	2.0E-27	rs147049568	downstream	-37017	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16290849	Mean corpuscular hemoglobin concentration,	8.0E-80	rs147049568	downstream	-37017	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
6:16290849	Mean corpuscular volume,	3.0E-55	rs147049568	downstream	-37017	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
6:16290849	Red cell distribution width,	6.0E-24	rs147049568	downstream	-37017	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
6:16290849	Immature fraction of reticulocytes,	5.0E-13	rs147049568	downstream	-37017	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
6:16290849	Reticulocyte count,	8.0E-35	rs147049568	downstream	-37017	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
6:16290849	Hemoglobin levels,	2.0E-9	rs147049568	downstream	-37017	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
6:16290849	Red blood cell count,	2.0E-12	rs147049568	downstream	-37017	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
6:16290849	High light scatter reticulocyte count,	6.0E-37	rs147049568	downstream	-37017	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
6:16290849	High light scatter reticulocyte percentage of red cells,	5.0E-32	rs147049568	downstream	-37017	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16290849	Red cell distribution width,	4.0E-13	rs147049568	downstream	-37017	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16290849	Reticulocyte count,	1.0E-27	rs147049568	downstream	-37017	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16290849	Reticulocyte fraction of red cells,	4.0E-34	rs147049568	downstream	-37017	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16290849	Mean corpuscular hemoglobin concentration,	7.0E-13	rs147049568	downstream	-37017	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16290849	Mean corpuscular hemoglobin,	3.0E-49	rs147049568	downstream	-37017	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16290849	Mean corpuscular volume,	5.0E-39	rs147049568	downstream	-37017	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16290862	Mean corpuscular volume,	4.0E-17	rs6926552	downstream	-37004	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16294722	Red blood cell count,	6.0E-23	rs7765828	downstream	-33144	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
6:16294722	Mean corpuscular hemoglobin,	9.0E-204	rs7765828	downstream	-33144	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
6:16294722	Red blood cell count,	5.0E-22	rs7765828	downstream	-33144	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
6:16294722	Mean corpuscular hemoglobin,	1.0E-186	rs7765828	downstream	-33144	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
6:16294722	Mean corpuscular volume,	4.0E-152	rs7765828	downstream	-33144	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
6:16294722	Mean corpuscular hemoglobin,	2.0E-160	rs7765828	downstream	-33144	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
6:16294722	QT interval,	3.0E-10	rs7765828	downstream	-33144	Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
6:16294722	Mean corpuscular hemoglobin,	4.0E-26	rs7765828	downstream	-33144	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16294722	Red blood cell count,	6.0E-17	rs7765828	downstream	-33144	A cross-population atlas of genetic associations for 220 human phenotypes.
6:16294722	Mean corpuscular volume,	1.0E-90	rs7765828	downstream	-33144	A cross-population atlas of genetic associations for 220 human phenotypes.
6:16294722	Mean corpuscular hemoglobin,	3.0E-139	rs7765828	downstream	-33144	A cross-population atlas of genetic associations for 220 human phenotypes.
6:16295348	Red blood cell count,	2.0E-9	rs142002554	downstream	-32518	A cross-population atlas of genetic associations for 220 human phenotypes.
6:16295348	Mean corpuscular volume,	2.0E-32	rs142002554	downstream	-32518	A cross-population atlas of genetic associations for 220 human phenotypes.
6:16295348	Mean corpuscular hemoglobin,	1.0E-42	rs142002554	downstream	-32518	A cross-population atlas of genetic associations for 220 human phenotypes.
6:16296824	General cognitive ability,	8.0E-9	rs180020	downstream	-31042	Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
6:16298971	Mean corpuscular hemoglobin,	2.0E-30	rs147840525	downstream	-28895	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
6:16298971	Mean corpuscular volume,	1.0E-23	rs147840525	downstream	-28895	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
6:16306751	Pulse pressure,	3.0E-8	rs16885	downstream	-21115	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
6:16310030	Cognitive performance (MTAG),	1.0E-8	rs180009	downstream	-17836	Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
6:16314031	Verbal-numerical reasoning,	2.0E-8	rs180002	downstream	-13835	A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data.
6:16315658	Self-reported math ability (MTAG),	2.0E-8	rs180001	downstream	-12208	Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
6:16315658	Highest math class taken (MTAG),	3.0E-8	rs180001	downstream	-12208	Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
6:16320987	General cognitive ability,	8.0E-10	rs179994	downstream	-6879	Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
6:16321792	Systolic blood pressure,	3.0E-11	rs179993	downstream	-6074	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
6:16322978	High light scatter reticulocyte percentage of red cells,	3.0E-12	rs557966248	downstream	-4888	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16322978	High light scatter reticulocyte count,	2.0E-11	rs557966248	downstream	-4888	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16322978	Reticulocyte fraction of red cells,	7.0E-14	rs557966248	downstream	-4888	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16322978	Reticulocyte count,	4.0E-12	rs557966248	downstream	-4888	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
6:16322978	Immature fraction of reticulocytes,	1.0E-9	rs557966248	downstream	-4888	The Polygenic and Monogenic Basis of Blood Traits and Diseases.
6:16324322	Systolic blood pressure,	1.0E-8	rs179992	downstream	-3544	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
6:16343056	Gambling,	5.0E-6	rs9383153	upstream	15190	Genome-wide association study of a quantitative disordered gambling trait.
6:16371545	Bilateral cleft lip,	4.0E-6	rs59728940	upstream	43679	The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip.

Position	HGVS	dbSNP id	Phenotype List	Distance	Clinvar Significance
6:16290530	NM_006877.4(GMPR):c.766T>A (p.Phe256Ile)	rs1042391	GMP REDUCTASE POLYMORPHISM\|not provided	-37336	Benign
6:16290742	NM_006877.4(GMPR):c.747G>A (p.Thr249=)	rs116633477	not provided	-37124	Benign
6:16290761	NM_006877.4(GMPR):c.766T>A (p.Phe256Ile)	rs1042391	GMP REDUCTASE POLYMORPHISM\|not provided	-37105	Benign
6:16290761	NM_006877.4(GMPR):c.766T>A (p.Phe256Ile)	rs1042391	GMP REDUCTASE POLYMORPHISM\|not provided	-37105	Benign
6:16290848	NM_006877.4(GMPR):c.855_856dup (p.Arg286fs)	rs147049568	not provided	-37018	Likely benign
6:16295278	NM_006877.4(GMPR):c.899A>T (p.Asp300Val)	rs78806162	not provided	-32588	Benign
6:16295347	NM_006877.4(GMPR):c.970_973dup (p.Lys325fs)	rs142002554	not provided	-32519	Benign
6:16306520	NM_001128164.2(ATXN1):c.2257C>T (p.Pro753Ser)	rs16885	not specified	-21346	Likely benign
6:16306751	NM_001128164.2(ATXN1):c.2257C>T (p.Pro753Ser)	rs16885	not specified	-21115	Likely benign
6:16306751	NM_001128164.2(ATXN1):c.2257C>T (p.Pro753Ser)	rs16885	not specified	-21115	Likely benign
6:16306858	NM_001128164.2(ATXN1):c.2150C>T (p.Ala717Val)	rs41267702	Spinocerebellar ataxia type 1\|not specified	-21008	Likely benign
6:16306865	NM_001128164.2(ATXN1):c.2143G>A (p.Gly715Ser)	rs149993107	not provided	-21001	Uncertain significance
6:16326611	NM_001128164.2(ATXN1):c.1917+14G>T	NA	not provided	-1255	Benign
6:16326738	NM_001128164.2(ATXN1):c.1804G>T (p.Ala602Ser)	rs1760808820	Spinocerebellar ataxia type 1	-1128	Uncertain significance
6:16326864	NM_001128164.2(ATXN1):c.1678G>A (p.Val560Met)	rs139918586	not provided	-1002	Uncertain significance
6:16326891	NM_001128164.2(ATXN1):c.1651C>T (p.Gln551Ter)	rs1554137844	not provided	-975	Uncertain significance
6:16326967	NM_001128164.2(ATXN1):c.1575C>T (p.Thr525=)	NA	not provided	-899	Likely benign
6:16326979	NM_001128164.2(ATXN1):c.1563G>C (p.Thr521=)	rs528819863	Toe walking	-887	Uncertain significance
6:16327099	NM_001128164.2(ATXN1):c.1212A>G (p.Glu404=)	rs2075974	not specified	-767	Likely benign
6:16327330	NM_001128164.2(ATXN1):c.1212A>G (p.Glu404=)	rs2075974	not specified	-536	Likely benign
6:16327330	NM_001128164.2(ATXN1):c.1212A>G (p.Glu404=)	rs2075974	not specified	-536	Likely benign
6:16327384	NM_001128164.2(ATXN1):c.927T>C (p.Ala309=)	rs179990	not specified	-482	Likely benign
6:16327384	NM_001128164.2(ATXN1):c.927T>G (p.Ala309=)	rs179990	not specified	-482	Likely benign
6:16327474	NM_001128164.2(ATXN1):c.1068C>A (p.Tyr356Ter)	NA	not provided	-392	Uncertain significance
6:16327615	NM_001128164.2(ATXN1):c.927T>G (p.Ala309=)	rs179990	not specified	-251	Likely benign
6:16327615	NM_001128164.2(ATXN1):c.927T>C (p.Ala309=)	rs179990	not specified	-251	Likely benign
6:16327615	NM_001128164.2(ATXN1):c.927T>G (p.Ala309=)	rs179990	not specified	-251	Likely benign
6:16327615	NM_001128164.2(ATXN1):c.927T>C (p.Ala309=)	rs179990	not specified	-251	Likely benign
6:16327636	NM_001128164.2(ATXN1):c.675G>C (p.Gln225His)	rs192671844	not specified	-230	Likely benign
6:16327666	NM_001128164.2(ATXN1):c.645G>T (p.Gln215His)	rs184327938	not specified	-200	Likely benign
6:16327672	NM_001128164.2(ATXN1):c.639G>T (p.Gln213His)	rs3817753	not specified	-194	Likely benign
6:16327675	NM_001128164.2(ATXN1):c.636G>T (p.Gln212His)	rs376233432	not specified	-191	Uncertain significance
6:16327676	NM_001128164.2(ATXN1):c.633_635del (p.His211del)	rs759132871	not specified	-190	Uncertain significance
6:16327678	NM_001128164.2(ATXN1):c.633T>G (p.His211Gln)	rs59310777	not specified	-188	Likely benign
6:16327681	NM_001128164.2(ATXN1):c.630G>T (p.Gln210His)	rs368218879	not specified	-185	Uncertain significance
6:16327684	NM_001128164.2(ATXN1):c.588GCA[14] (p.Gln208dup)	rs193922926	not specified\|Spinocerebellar ataxia type 1	-182	Benign/Likely benign
6:16327685	NM_001128164.2(ATXN1):c.588GCA[12] (p.Gln208del)	rs193922926	not specified\|not provided	-181	Uncertain significance
6:16327687	NM_000332.3(ATXN1):c.589_591CAG(36_38) (p.Gln208_His209insGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGln)	rs193922926	Spinocerebellar ataxia type 1	-179	Pathogenic
6:16327687	NM_001128164.2(ATXN1):c.624G>T (p.Gln208His)	rs28555263	not specified	-179	Uncertain significance
6:16327690	NM_001128164.2(ATXN1):c.621G>T (p.Gln207His)	rs201030692	not specified\|Spinocerebellar ataxia type 1	-176	Conflicting interpretations of pathogenicity
6:16327770	NM_001128164.2(ATXN1):c.772G>T (p.Gly258Cys)	NA	Toe walking	-96	Likely pathogenic
6:16327837	NM_001128164.2(ATXN1):c.474A>G (p.Ala158=)	rs2072736	not specified\|not provided	-29	Benign
6:16327864	NM_001128164.2(ATXN1):c.636GCA[16] (p.Gln224_Gln225dup)	rs751421308	Spinocerebellar ataxia type 1\|not specified	-2	Benign
6:16327864	NM_001128164.2(ATXN1):c.636GCA[15] (p.Gln225dup)	NA	not specified\|not provided	-2	Benign/Likely benign
6:16327865	NM_001128164.2(ATXN1):c.636GCA[12] (p.Gln224_Gln225del)	NA	not provided	-1	Likely benign
6:16327867	NM_001128164.2(ATXN1):c.675G>C (p.Gln225His)	rs192671844	not specified	1	Likely benign
6:16327867	NM_001128164.2(ATXN1):c.675G>C (p.Gln225His)	rs192671844	not specified	1	Likely benign
6:16327897	NM_001128164.2(ATXN1):c.645G>T (p.Gln215His)	rs184327938	not specified	31	Likely benign
6:16327897	NM_001128164.2(ATXN1):c.645G>T (p.Gln215His)	rs184327938	not specified	31	Likely benign
6:16327903	NM_001128164.2(ATXN1):c.639G>T (p.Gln213His)	rs3817753	not specified	37	Likely benign
6:16327903	NM_001128164.2(ATXN1):c.639G>T (p.Gln213His)	rs3817753	not specified	37	Likely benign
6:16327906	NM_001128164.2(ATXN1):c.636G>T (p.Gln212His)	rs376233432	not specified	40	Uncertain significance
6:16327906	NM_001128164.2(ATXN1):c.636G>T (p.Gln212His)	rs376233432	not specified	40	Uncertain significance
6:16327907	NM_001128164.2(ATXN1):c.633_635del (p.His211del)	rs759132871	not specified	41	Uncertain significance
6:16327907	NM_001128164.2(ATXN1):c.633_635del (p.His211del)	rs759132871	not specified	41	Uncertain significance
6:16327909	NM_001128164.2(ATXN1):c.633T>G (p.His211Gln)	rs59310777	not specified	43	Likely benign
6:16327909	NM_001128164.2(ATXN1):c.633T>G (p.His211Gln)	rs59310777	not specified	43	Likely benign
6:16327912	NM_001128164.2(ATXN1):c.630G>T (p.Gln210His)	rs368218879	not specified	46	Uncertain significance
6:16327912	NM_001128164.2(ATXN1):c.630G>T (p.Gln210His)	rs368218879	not specified	46	Uncertain significance
6:16327915	NM_001128164.2(ATXN1):c.588GCA[14] (p.Gln208dup)	rs193922926	not specified\|Spinocerebellar ataxia type 1	49	Benign/Likely benign
6:16327915	NM_001128164.2(ATXN1):c.588GCA[14] (p.Gln208dup)	rs193922926	not specified\|Spinocerebellar ataxia type 1	49	Benign/Likely benign
6:16327915	NM_001128164.2(ATXN1):c.627T>G (p.His209Gln)	NA	not provided	49	Uncertain significance
6:16327916	NM_001128164.2(ATXN1):c.588GCA[12] (p.Gln208del)	rs193922926	not specified\|not provided	50	Uncertain significance
6:16327916	NM_001128164.2(ATXN1):c.588GCA[12] (p.Gln208del)	rs193922926	not specified\|not provided	50	Uncertain significance
6:16327918	NM_000332.3(ATXN1):c.589_591CAG(36_38) (p.Gln208_His209insGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGln)	rs193922926	Spinocerebellar ataxia type 1	52	Pathogenic
6:16327918	NM_001128164.2(ATXN1):c.624G>T (p.Gln208His)	rs28555263	not specified	52	Uncertain significance
6:16327918	NM_000332.3(ATXN1):c.589_591CAG(36_38) (p.Gln208_His209insGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGln)	rs193922926	Spinocerebellar ataxia type 1	52	Pathogenic
6:16327918	NM_001128164.2(ATXN1):c.624G>T (p.Gln208His)	rs28555263	not specified	52	Uncertain significance
6:16327921	NM_001128164.2(ATXN1):c.621G>T (p.Gln207His)	rs201030692	not specified\|Spinocerebellar ataxia type 1	55	Conflicting interpretations of pathogenicity
6:16327921	NM_001128164.2(ATXN1):c.621G>T (p.Gln207His)	rs201030692	not specified\|Spinocerebellar ataxia type 1	55	Conflicting interpretations of pathogenicity
6:16327933	NM_001128164.2(ATXN1):c.609G>T (p.Gln203His)	rs199744696	Spinocerebellar ataxia type 1	67	Likely benign
6:16327986	NM_001128164.2(ATXN1):c.556A>T (p.Ser186Cys)	NA	not provided	120	Likely benign
6:16328068	NM_001128164.2(ATXN1):c.474A>G (p.Ala158=)	rs2072736	not specified\|not provided	202	Benign
6:16328068	NM_001128164.2(ATXN1):c.474A>G (p.Ala158=)	rs2072736	not specified\|not provided	202	Benign
6:16328447	NM_001128164.2(ATXN1):c.95C>G (p.Thr32Ser)	NA	not provided	581	Likely benign
6:16348584	GRCh37/hg19 6p22.3(chr6:16348584-16559316)	NA	not specified	20718	Likely pathogenic
6:16350981	GRCh37/hg19 6p22.3(chr6:16350981-16598133)x1	NA	See cases	23115	Likely benign

Position	Type	Class	Distance	Location with respect to STR
6:16326006-16326162	FAM	SINE	-1860	downstream
6:16328889-16329187	AluSc8	SINE	1023	upstream

Position	Population	BlockLength (kb)	Distance	Location with respect to STR	No. of SNPs	SNPs in the Haploblock
6:16285256-16285264	all_pop	0.009	-42610	downstream	2	rs78131658, rs54135553,
6:16285256-16285264	AMR	0.009	-42610	downstream	2	rs78131658, rs54135553,
6:16285256-16285264	EAS	0.009	-42610	downstream	2	rs78131658, rs54135553,
6:16285256-16285264	SAS	0.009	-42610	downstream	2	rs78131658, rs54135553,
6:16285264-16288943	EUR	3.68	-42602	downstream	5	rs541355532, rs6459467, rs2327958, rs71554562, rs11464393,
6:16285886-16289908	AMR	4.023	-41980	downstream	14	rs140768059, rs55759663, rs6459467, rs2327958, rs71554562, rs114643938, rs34091725, rs180025, rs9350003, rs11969354, rs180024, rs11969405, rs79989301, rs7153507,
6:16286516-16289417	AFR	2.902	-41350	downstream	12	rs80155234, rs55759663, rs75175757, rs73362657, rs6459467, rs11968694, rs2327958, rs150391356, rs34091725, rs11969354, rs9477077, rs8005694,
6:16287211-16289908	all_pop	2.698	-40655	downstream	12	rs55759663, rs6459467, rs2327958, rs114643938, rs34091725, rs9350003, rs11969354, rs9477077, rs11969405, rs9477078, rs79989301, rs7153507,
6:16287211-16289908	EAS	2.698	-40655	downstream	6	rs55759663, rs6459467, rs2327958, rs114643938, rs9350003, rs7153507,
6:16287211-16289908	SAS	2.698	-40655	downstream	12	rs55759663, rs73362657, rs6459467, rs2327958, rs114643938, rs34091725, rs9350003, rs11969354, rs11969405, rs71554563, rs79989301, rs7153507,
6:16289075-16289971	EUR	0.897	-38791	downstream	8	rs34091725, rs9350003, rs11969354, rs11969405, rs71554563, rs79989301, rs71535075, rs7099931,
6:16289538-16290003	AFR	0.466	-38328	downstream	6	rs11969405, rs9477078, rs79989301, rs111737251, rs71535075, rs947707,
6:16290761-16295038	all_pop	4.278	-37105	downstream	10	rs1042391, rs6926552, rs4716057, rs4716058, rs74802377, rs79626813, rs4716059, rs9350004, rs7765828, rs1321595,
6:16290761-16295038	AMR	4.278	-37105	downstream	10	rs1042391, rs6926552, rs4716057, rs4716058, rs74802377, rs79626813, rs4716059, rs9350004, rs7765828, rs1321595,
6:16290761-16294722	EAS	3.962	-37105	downstream	3	rs1042391, rs9350004, rs776582,
6:16290761-16295038	EUR	4.278	-37105	downstream	10	rs1042391, rs6926552, rs4716057, rs4716058, rs74802377, rs79626813, rs4716059, rs9350004, rs7765828, rs1321595,
6:16290761-16295038	SAS	4.278	-37105	downstream	13	rs1042391, rs6926552, rs4716057, rs4716058, rs74802377, rs79626813, rs4716059, rs73362663, rs9350004, rs372171309, rs73724825, rs7765828, rs1321595,
6:16290862-16295028	AFR	4.167	-37004	downstream	12	rs6926552, rs4716057, rs4716058, rs74802377, rs79626813, rs4716059, rs73362663, rs73724824, rs73724825, rs7765828, rs78609940, rs7372482,
6:16295482-16295555	AFR	0.074	-32384	downstream	2	rs77813716, rs104242,
6:16295861-16296677	all_pop	0.817	-32005	downstream	2	rs180022, rs7336266,
6:16296677-16297420	AFR	0.744	-31189	downstream	2	rs73362668, rs6075953,
6:16296677-16296824	AMR	0.148	-31189	downstream	3	rs73362668, rs180021, rs18002,
6:16296677-16297420	EAS	0.744	-31189	downstream	2	rs73362668, rs6075953,
6:16296707-16296824	all_pop	0.118	-31159	downstream	2	rs180021, rs18002,
6:16296707-16296824	EUR	0.118	-31159	downstream	2	rs180021, rs18002,
6:16296707-16296824	SAS	0.118	-31159	downstream	2	rs180021, rs18002,
6:16297715-16300824	all_pop	3.11	-30151	downstream	7	rs180019, rs34616273, rs2237225, rs138233584, rs148689787, rs56404385, rs1687781,
6:16297715-16300824	AMR	3.11	-30151	downstream	7	rs180019, rs34616273, rs2237225, rs138233584, rs148689787, rs56404385, rs1687781,
6:16297715-16306202	EAS	8.488	-30151	downstream	10	rs180019, rs2237225, rs138233584, rs148689787, rs78566245, rs56404385, rs16877817, rs66843340, rs73362674, rs18001,
6:16297715-16298618	EUR	0.904	-30151	downstream	2	rs180019, rs3461627,
6:16297715-16300771	SAS	3.057	-30151	downstream	5	rs180019, rs34616273, rs2237225, rs138233584, rs5640438,
6:16298180-16300824	AFR	2.645	-29686	downstream	9	rs60925045, rs9477080, rs34616273, rs2237225, rs145816850, rs138233584, rs138168106, rs56404385, rs1687781,
6:16300824-16301316	EUR	0.493	-27042	downstream	2	rs16877817, rs6684334,
6:16303597-16306074	all_pop	2.478	-24269	downstream	2	rs11453731, rs7336267,
6:16303597-16310644	AMR	7.048	-24269	downstream	15	rs11453731, rs73362674, rs180017, rs111168, rs2072737, rs180015, rs9396662, rs542289170, rs570511221, rs199934662, rs60352927, rs180010, rs180009, rs4716060, rs7752728,
6:16303597-16306359	EUR	2.763	-24269	downstream	3	rs11453731, rs180017, rs11116,
6:16304322-16307853	AFR	3.532	-23544	downstream	12	rs72840230, rs72840232, rs3840417, rs16877822, rs73362674, rs180017, rs2072737, rs111476258, rs180015, rs56171990, rs542289170, rs11136608,
6:16306074-16306202	SAS	0.129	-21792	downstream	2	rs73362674, rs18001,
6:16306204-16307853	all_pop	1.65	-21662	downstream	8	rs3116712, rs111168, rs2072737, rs180015, rs9396662, rs56171990, rs542289170, rs11136608,
6:16306359-16307853	SAS	1.495	-21507	downstream	7	rs111168, rs2072737, rs180015, rs9396662, rs56171990, rs542289170, rs11136608,
6:16306866-16307743	EAS	0.878	-21000	downstream	4	rs2072737, rs180015, rs9396662, rs54228917,
6:16307871-16307906	SAS	0.036	-19995	downstream	2	rs186523000, rs57051122,
6:16308105-16310885	AFR	2.781	-19761	downstream	12	rs11970452, rs146094409, rs9464878, rs199934662, rs60352927, rs72840234, rs9477081, rs180010, rs202094433, rs4716060, rs112839209, rs431741,
6:16308105-16308449	EAS	0.345	-19761	downstream	2	rs11970452, rs946487,
6:16308449-16310885	all_pop	2.437	-19417	downstream	8	rs9464878, rs199934662, rs60352927, rs180010, rs180009, rs4716060, rs112839209, rs431741,
6:16308552-16311958	EAS	3.407	-19314	downstream	6	rs199934662, rs142981911, rs60352927, rs4716060, rs4317413, rs13968193,
6:16308552-16311958	SAS	3.407	-19314	downstream	9	rs199934662, rs60352927, rs180010, rs180009, rs4716060, rs77527285, rs112839209, rs4317413, rs13968193,
6:16309960-16310456	EUR	0.497	-17906	downstream	3	rs180010, rs180009, rs471606,
6:16313052-16313057	AFR	0.006	-14814	downstream	2	rs529347964, rs18000,
6:16313057-16324322	EUR	11.266	-14809	downstream	23	rs180004, rs180003, rs180002, rs74800515, rs6901150, rs113193263, rs180001, rs61075502, rs180000, rs72630, rs179998, rs179997, rs179996, rs179995, rs141382123, rs179994, rs2038018, rs56336401, rs179993, rs2237224, rs909522, rs2073519, rs17999,
6:16313932-16315658	AFR	1.727	-13934	downstream	8	rs180003, rs6901150, rs12661684, rs113193263, rs79307303, rs76177153, rs111632785, rs18000,
6:16313932-16316882	all_pop	2.951	-13934	downstream	8	rs180003, rs180002, rs6901150, rs12661684, rs113193263, rs180001, rs61075502, rs18000,
6:16313932-16318588	SAS	4.657	-13934	downstream	11	rs180003, rs180002, rs6901150, rs12661684, rs113193263, rs180001, rs61075502, rs180000, rs72630, rs61689184, rs17999,
6:16314031-16325510	AMR	11.48	-13835	downstream	28	rs180002, rs6901150, rs12661684, rs113193263, rs180001, rs61075502, rs180000, rs72630, rs61689184, rs179998, rs179997, rs179996, rs179995, rs1886349, rs141382123, rs179994, rs9383152, rs2038018, rs56336401, rs179993, rs2237224, rs909522, rs2073519, rs179992, rs7765262, rs5874552, rs11326648, rs228284,
6:16314031-16324322	EAS	10.292	-13835	downstream	24	rs180002, rs6901150, rs12661684, rs113193263, rs180001, rs61075502, rs180000, rs72630, rs61689184, rs179998, rs179997, rs179996, rs179995, rs1886349, rs141382123, rs179994, rs9383152, rs2038018, rs56336401, rs179993, rs2237224, rs909522, rs2073519, rs17999,
6:16315947-16320223	AFR	4.277	-11919	downstream	17	rs61075502, rs112203139, rs114384998, rs116527646, rs116079497, rs72630, rs78375753, rs146789972, rs111298421, rs56785042, rs61689184, rs113006530, rs76907939, rs179998, rs179996, rs179995, rs11216782,
6:16317062-16318588	all_pop	1.527	-10804	downstream	3	rs72630, rs61689184, rs17999,
6:16318633-16326587	all_pop	7.955	-9233	downstream	23	rs179997, rs179996, rs179995, rs1886349, rs141382123, rs179994, rs2038018, rs56336401, rs179993, rs2237224, rs909522, rs2073519, rs179992, rs7765262, rs5874552, rs11326648, rs2282847, rs179991, rs72653742, rs2282844, rs3216220, rs60084677, rs7811524,
6:16318633-16326587	SAS	7.955	-9233	downstream	23	rs179997, rs179996, rs179995, rs1886349, rs141382123, rs179994, rs2038018, rs56336401, rs179993, rs2237224, rs909522, rs2073519, rs179992, rs7765262, rs5874552, rs11326648, rs2282847, rs179991, rs72653742, rs2282844, rs3216220, rs60084677, rs7811524,
6:16320320-16327330	AFR	7.011	-7546	downstream	22	rs1886349, rs141382123, rs179994, rs2038018, rs56336401, rs2237224, rs909522, rs2073519, rs73724832, rs113176122, rs7765262, rs5874552, rs11326648, rs2282847, rs179991, rs72653742, rs2282844, rs3216220, rs60084677, rs73724833, rs72840240, rs207597,
6:16324451-16327330	EAS	2.88	-3415	downstream	11	rs7765262, rs5874552, rs11326648, rs2282847, rs179991, rs72653742, rs2282844, rs3216220, rs60084677, rs78115249, rs207597,
6:16324451-16327330	EUR	2.88	-3415	downstream	11	rs7765262, rs5874552, rs11326648, rs2282847, rs179991, rs72653742, rs2282844, rs3216220, rs60084677, rs78115249, rs207597,
6:16325562-16327330	AMR	1.769	-2304	downstream	7	rs179991, rs72653742, rs2282844, rs3216220, rs60084677, rs78115249, rs207597,
6:16327909-16327918	all_pop	0.01	43	upstream	2	rs59310777, rs2855526,
6:16327918-16328068	AFR	0.151	52	upstream	2	rs28555263, rs207273,
6:16327918-16332744	AMR	4.827	52	upstream	10	rs28555263, rs2072736, rs6938433, rs9358089, rs9370887, rs2237223, rs142517, rs200409591, rs2073518, rs207351,
6:16327918-16335623	EAS	7.706	52	upstream	12	rs28555263, rs2072736, rs6938433, rs9358089, rs9370887, rs2237223, rs142517, rs200409591, rs2073518, rs2073517, rs9370888, rs3408865,
6:16327918-16335623	SAS	7.706	52	upstream	13	rs28555263, rs2072736, rs6938433, rs9358089, rs9370887, rs2237223, rs142517, rs200409591, rs2073518, rs2073517, rs179989, rs9370888, rs3408865,
6:16328068-16335623	all_pop	7.556	202	upstream	12	rs2072736, rs6938433, rs9358089, rs9370887, rs2237223, rs142517, rs200409591, rs2073518, rs2073517, rs179989, rs9370888, rs3408865,
6:16328938-16337374	AFR	8.437	1072	upstream	15	rs6938433, rs9358089, rs9370887, rs74744439, rs2237223, rs2073518, rs2073517, rs16877885, rs179989, rs56981561, rs9370888, rs73724835, rs72840241, rs7753715, rs5624453,
6:16328938-16332730	EUR	3.793	1072	upstream	5	rs6938433, rs9358089, rs9370887, rs142517, rs207351,
6:16334419-16348883	AMR	14.465	6553	upstream	21	rs179989, rs9370888, rs34088655, rs179988, rs13207978, rs7749925, rs71554573, rs9383153, rs9367911, rs179986, rs2016498, rs90671, rs9370890, rs6916034, rs12660858, rs9367912, rs6916602, rs6937740, rs9358090, rs179984, rs939666,
6:16335623-16338904	EUR	3.282	7757	upstream	3	rs34088655, rs179988, rs1320797,
6:16337374-16338904	all_pop	1.531	9508	upstream	3	rs56244538, rs179988, rs1320797,
6:16338221-16348883	SAS	10.663	10355	upstream	18	rs179988, rs13207978, rs7749925, rs71554573, rs9383153, rs9367911, rs179986, rs2016498, rs90671, rs9370890, rs6916034, rs12660858, rs9367912, rs6916602, rs6937740, rs9358090, rs179984, rs939666,
6:16338904-16350838	AFR	11.935	11038	upstream	38	rs13207978, rs114264388, rs60968679, rs7749925, rs74729778, rs112876660, rs71554573, rs78085193, rs57791752, rs9383153, rs61267105, rs9367911, rs73364711, rs73724840, rs56178525, rs6914035, rs179986, rs115665760, rs2016498, rs73724841, rs9370890, rs114598241, rs6916034, rs12660858, rs9367912, rs114308848, rs6916602, rs6937740, rs56792852, rs72840246, rs9358090, rs59747547, rs9396665, rs72840247, rs61312254, rs112246571, rs56175042, rs11188423,
6:16338904-16344914	EAS	6.011	11038	upstream	7	rs13207978, rs7749925, rs74729778, rs71554573, rs9383153, rs9367911, rs201649,
6:16340776-16342574	all_pop	1.799	12910	upstream	2	rs7749925, rs7155457,
6:16343056-16343593	all_pop	0.538	15190	upstream	2	rs9383153, rs936791,
6:16343056-16343593	EUR	0.538	15190	upstream	2	rs9383153, rs936791,
6:16344692-16347211	all_pop	2.52	16826	upstream	5	rs179986, rs2016498, rs90671, rs79465944, rs937089,
6:16344692-16351420	EUR	6.729	16826	upstream	11	rs179986, rs2016498, rs90671, rs79465944, rs179985, rs6916034, rs12660858, rs6916602, rs179984, rs9396665, rs11632514,
6:16345398-16346276	EAS	0.879	17532	upstream	2	rs90671, rs7946594,
6:16347100-16348728	EAS	1.629	19234	upstream	8	rs149233199, rs9370890, rs6916034, rs12660858, rs9367912, rs6916602, rs6937740, rs935809,
6:16347494-16347505	all_pop	0.012	19628	upstream	2	rs6916034, rs1266085,
6:16347525-16348728	all_pop	1.204	19659	upstream	4	rs9367912, rs6916602, rs6937740, rs935809,
6:16348869-16351601	all_pop	2.733	21003	upstream	6	rs179984, rs9396665, rs75457709, rs111884236, rs9464880, rs11177339,
6:16348869-16348928	EAS	0.06	21003	upstream	3	rs179984, rs9396665, rs7545770,
6:16351129-16351601	AFR	0.473	23263	upstream	3	rs72840248, rs9464880, rs11177339,
6:16351692-16362692	AMR	11.001	23826	upstream	14	rs34183749, rs11285936, rs148487913, rs179981, rs179980, rs179979, rs179978, rs179977, rs179976, rs11969836, rs179975, rs179974, rs179973, rs17997,
6:16353828-16358358	all_pop	4.531	25962	upstream	7	rs9477087, rs9477088, rs11285936, rs57015402, rs962998, rs148487913, rs17998,
6:16354287-16360049	AFR	5.763	26421	upstream	10	rs9477088, rs9464881, rs80115059, rs11285936, rs962998, rs148487913, rs179980, rs179976, rs73724842, rs691450,
6:16355791-16359021	EAS	3.231	27925	upstream	5	rs11285936, rs57015402, rs962998, rs148487913, rs17997,
6:16355791-16371544	EUR	15.754	27925	upstream	27	rs11285936, rs148487913, rs179981, rs179980, rs179979, rs179978, rs179977, rs179976, rs11969836, rs179975, rs179974, rs179973, rs179972, rs179971, rs179970, rs179969, rs3216219, rs56355703, rs179968, rs179967, rs35476061, rs34627413, rs179966, rs179965, rs179964, rs179962, rs5972894,
6:16355791-16357042	SAS	1.252	27925	upstream	3	rs11285936, rs57015402, rs96299,
6:16357463-16365044	SAS	7.582	29597	upstream	21	rs148487913, rs179981, rs179980, rs179979, rs179978, rs179977, rs179976, rs11969836, rs179975, rs179974, rs179973, rs2237221, rs179972, rs179971, rs179970, rs179969, rs3216219, rs56355703, rs179968, rs179967, rs3547606,
6:16358679-16360049	all_pop	1.371	30813	upstream	6	rs179980, rs179979, rs179978, rs179977, rs179976, rs691450,
6:16360246-16360323	EAS	0.078	32380	upstream	3	rs11969836, rs78330169, rs17997,
6:16360299-16360323	AFR	0.025	32433	upstream	2	rs78330169, rs17997,
6:16361337-16365286	AFR	3.95	33471	upstream	16	rs116412685, rs179974, rs179973, rs179971, rs58095172, rs179970, rs179969, rs3216219, rs56355703, rs58936812, rs9477091, rs179968, rs179967, rs35476061, rs56997662, rs3462741,
6:16362246-16366366	all_pop	4.121	34380	upstream	21	rs179974, rs179973, rs2237221, rs179972, rs179971, rs58095172, rs179970, rs179969, rs3216219, rs56355703, rs58936812, rs9477091, rs179968, rs179967, rs35476061, rs56997662, rs34627413, rs60852545, rs179966, rs179965, rs17996,
6:16362388-16367976	EAS	5.589	34522	upstream	18	rs179973, rs2237221, rs179972, rs179971, rs3216219, rs56355703, rs79963215, rs179968, rs74194628, rs34627413, rs60852545, rs75396966, rs76484837, rs139217038, rs540955323, rs553875418, rs574017741, rs56295497,
6:16362742-16366366	AMR	3.625	34876	upstream	12	rs179971, rs179970, rs179969, rs3216219, rs56355703, rs179968, rs179967, rs35476061, rs34627413, rs179966, rs179965, rs17996,
6:16365326-16368175	SAS	2.85	37460	upstream	5	rs60852545, rs179966, rs179965, rs179964, rs17996,
6:16367226-16370002	AFR	2.777	39360	upstream	14	rs145287971, rs78844305, rs74737314, rs200684193, rs76484837, rs139217038, rs540955323, rs553875418, rs574017741, rs562954973, rs71658367, rs9477093, rs9477094, rs7917714,
6:16367757-16367943	all_pop	0.187	39891	upstream	5	rs76484837, rs139217038, rs540955323, rs553875418, rs57401774,
6:16368758-16371088	all_pop	2.331	40892	upstream	3	rs71658367, rs9477093, rs5957296,
6:16371544-16372858	EAS	1.315	43678	upstream	3	rs59728940, rs179961, rs7429171,
6:16372061-16373072	AFR	1.012	44195	upstream	2	rs179961, rs14516387,
6:16372061-16372858	all_pop	0.798	44195	upstream	2	rs179961, rs7429171,
6:16372061-16373306	AMR	1.246	44195	upstream	3	rs179961, rs71717905, rs693423,
6:16372061-16373306	EUR	1.246	44195	upstream	3	rs179961, rs71717905, rs693423,
6:16372061-16373219	SAS	1.159	44195	upstream	3	rs179961, rs74291718, rs7171790,
6:16373169-16373173	AFR	0.005	45303	upstream	2	rs4590274, rs20213573,
6:16373219-16373938	AFR	0.72	45353	upstream	3	rs71717905, rs6934233, rs938315,
6:16373306-16373938	all_pop	0.633	45440	upstream	2	rs6934233, rs938315,
6:16374506-16374947	all_pop	0.442	46640	upstream	2	rs9396666, rs1319310,
6:16374506-16374947	SAS	0.442	46640	upstream	2	rs9396666, rs1319310,
6:16374947-16378554	EAS	3.608	47081	upstream	6	rs13193106, rs2237219, rs2237218, rs2237217, rs2282843, rs1321816,
6:16375252-16376950	all_pop	1.699	47386	upstream	4	rs2237219, rs2237218, rs2237217, rs17995,
6:16375252-16376624	AMR	1.373	47386	upstream	3	rs2237219, rs2237218, rs223721,
6:16375252-16377889	EUR	2.638	47386	upstream	6	rs2237219, rs2237218, rs2237217, rs179959, rs2282843, rs218836,
6:16375252-16378554	SAS	3.303	47386	upstream	7	rs2237219, rs2237218, rs2237217, rs179959, rs2282843, rs2188369, rs1321816,
6:16376162-16376624	AFR	0.463	48296	upstream	2	rs2237218, rs223721,
6:16377235-16377613	AFR	0.379	49369	upstream	2	rs150649488, rs228284,
6:16377647-16386025	AFR	8.379	49781	upstream	36	rs9477096, rs2188369, rs111875611, rs13218161, rs200062366, rs11965878, rs9477097, rs9477098, rs75670595, rs78573290, rs7745262, rs74734737, rs7774332, rs13437167, rs881405, rs876607, rs6935573, rs932295, rs9477101, rs9477102, rs6920318, rs6920639, rs4716064, rs7738608, rs75406553, rs7758453, rs7741594, rs2282842, rs9464882, rs9464883, rs78742717, rs9477104, rs10949352, rs10949353, rs143487285, rs7372484,

Conservation score was not calculated