Variant report

Variant	rs1341739
Chromosome Location	chr9:15847097-15847098
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 149 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:136)

rs_ID	r²[population]
rs10429512	1.00[CHD][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs10732334	1.00[YRI][hapmap]
rs10810445	1.00[YRI][hapmap]
rs10810447	1.00[YRI][hapmap]
rs1081243	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1081244	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1081246	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1081247	1.00[CEU][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1169469	0.87[EUR][1000 genomes]
rs1169470	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs1169471	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs1169472	1.00[CEU][hapmap];0.90[TSI][hapmap];0.91[EUR][1000 genomes]
rs1169474	0.87[EUR][1000 genomes]
rs1169475	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1169476	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1169477	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs1169481	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1177610	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs1177611	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs1184568	1.00[CEU][hapmap];0.83[LWK][hapmap];0.86[MEX][hapmap];0.90[TSI][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1184913	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1185652	0.82[EUR][1000 genomes]
rs1186048	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1186387	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs1328281	0.87[EUR][1000 genomes]
rs1341733	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs1361607	0.96[EUR][1000 genomes]
rs1361608	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1417976	1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs1572977	1.00[ASN][1000 genomes]
rs1578556	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1578557	0.93[EUR][1000 genomes]
rs1578558	1.00[CEU][hapmap];0.90[TSI][hapmap];0.93[EUR][1000 genomes]
rs1582200	0.93[EUR][1000 genomes]
rs1752777	0.86[EUR][1000 genomes]
rs1773046	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1773062	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1815697	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1832818	1.00[ASN][1000 genomes]
rs1891209	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs1935220	0.83[EUR][1000 genomes]
rs1935221	1.00[CEU][hapmap];0.82[TSI][hapmap];0.87[EUR][1000 genomes]
rs1935223	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs1954220	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2094519	1.00[CEU][hapmap]
rs2094520	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs2096119	1.00[YRI][hapmap]
rs2105313	0.87[EUR][1000 genomes]
rs2105314	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs2105320	1.00[ASN][1000 genomes]
rs2149230	0.81[EUR][1000 genomes]
rs2153724	1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs2182934	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs2182935	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2185664	1.00[YRI][hapmap]
rs2769714	0.87[EUR][1000 genomes]
rs2769716	0.88[EUR][1000 genomes]
rs2794624	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs2794625	1.00[CEU][hapmap];0.80[TSI][hapmap];0.87[EUR][1000 genomes]
rs2794626	0.87[EUR][1000 genomes]
rs2794627	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs2794628	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs2794629	0.87[EUR][1000 genomes]
rs2794631	0.82[EUR][1000 genomes]
rs2794632	0.81[EUR][1000 genomes]
rs2794638	0.82[EUR][1000 genomes]
rs2987045	0.85[EUR][1000 genomes]
rs2987046	0.81[EUR][1000 genomes]
rs2987053	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs2987054	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs2987057	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2987060	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs2987061	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs2987065	0.85[TSI][hapmap];0.81[EUR][1000 genomes]
rs2995024	0.86[EUR][1000 genomes]
rs2995025	0.84[EUR][1000 genomes]
rs3008683	0.80[EUR][1000 genomes]
rs3008691	1.00[CEU][hapmap]
rs3008692	0.81[EUR][1000 genomes]
rs3008693	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs3008695	0.81[EUR][1000 genomes]
rs3008698	1.00[CEU][hapmap]
rs3008700	0.80[EUR][1000 genomes]
rs4146288	1.00[ASN][1000 genomes]
rs4146289	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs4146292	1.00[YRI][hapmap]
rs4741544	1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6474973	1.00[YRI][hapmap]
rs6474976	1.00[ASN][1000 genomes]
rs6474977	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs6474978	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6474979	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7027040	1.00[ASN][1000 genomes]
rs7028328	0.92[EUR][1000 genomes]
rs7039881	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs7388793	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs7468716	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs770190	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs770192	0.89[EUR][1000 genomes]
rs770193	1.00[CEU][hapmap];1.00[CHD][hapmap];0.83[LWK][hapmap];0.86[MEX][hapmap];0.90[TSI][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs770194	1.00[CEU][hapmap];0.86[TSI][hapmap];0.89[EUR][1000 genomes]
rs770195	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs770196	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs770197	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs770198	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs770199	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs770200	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs770201	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs770202	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs770203	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs770204	1.00[CEU][hapmap];0.86[TSI][hapmap];0.88[EUR][1000 genomes]
rs770205	1.00[CEU][hapmap];0.86[TSI][hapmap];0.88[EUR][1000 genomes]
rs770206	1.00[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs770207	0.83[EUR][1000 genomes]
rs770210	0.82[EUR][1000 genomes]
rs770212	0.82[EUR][1000 genomes]
rs770214	0.82[EUR][1000 genomes]
rs770217	0.85[EUR][1000 genomes]
rs770218	0.82[EUR][1000 genomes]
rs7856877	0.89[EUR][1000 genomes]
rs7860354	0.93[EUR][1000 genomes]
rs7860463	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7860856	0.83[EUR][1000 genomes]
rs7861105	0.81[EUR][1000 genomes]
rs7865141	1.00[ASN][1000 genomes]
rs7865391	1.00[YRI][hapmap]
rs7874094	1.00[YRI][hapmap]
rs809493	0.84[EUR][1000 genomes]
rs9406543	1.00[ASN][1000 genomes]
rs9406544	1.00[ASN][1000 genomes]
rs9406546	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9407664	0.94[EUR][1000 genomes]
rs9407665	0.94[EUR][1000 genomes]
rs9407668	0.91[EUR][1000 genomes]
rs954932	1.00[YRI][hapmap]
rs955193	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv892627	chr9:15397969-15909450	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv892632	chr9:15590116-15869845	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv892633	chr9:15604746-15889411	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv892635	chr9:15731775-15876507	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv528964	chr9:15760822-15875162	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv892636	chr9:15794858-15876507	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv613666	chr9:15823667-15875162	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv613667	chr9:15823667-15876507	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv1016226	chr9:15841107-15875321	ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1015435	chr9:15841107-15880385	Enhancers ZNF genes & repeats Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv1032081	chr9:15845902-15878115	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv1027790	chr9:15845902-15878841	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15830200-15857200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr9:15844800-15850400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr9:15845000-15858800	Weak transcription	Thymus	Thymus
4	chr9:15846600-15847200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr9:15846600-15847200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr9:15846600-15847200	Enhancers	Brain Angular Gyrus	brain
7	chr9:15847000-15849000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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