Variant report

Variant	rs2987053
Chromosome Location	chr9:15909082-15909083
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 135 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:133)

rs_ID	r²[population]
rs1081243	0.87[EUR][1000 genomes]
rs1081244	0.84[EUR][1000 genomes]
rs1081246	0.87[EUR][1000 genomes]
rs1081247	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1169469	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1169470	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs1169471	1.00[CEU][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1169472	1.00[CEU][hapmap];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1169474	0.85[EUR][1000 genomes]
rs1169475	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1169476	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1169477	1.00[CEU][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1169481	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1169482	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][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];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1184913	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1185652	0.86[EUR][1000 genomes]
rs1186048	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1186387	1.00[CEU][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1328281	0.85[EUR][1000 genomes]
rs1328285	0.92[ASN][1000 genomes]
rs1341733	1.00[CEU][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1341739	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs1361607	0.82[EUR][1000 genomes]
rs1361608	0.82[EUR][1000 genomes]
rs1578556	0.82[EUR][1000 genomes]
rs1578557	0.83[EUR][1000 genomes]
rs1578558	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs1582200	0.83[EUR][1000 genomes]
rs16933738	1.00[ASN][1000 genomes]
rs1752777	0.84[EUR][1000 genomes]
rs1773046	0.85[EUR][1000 genomes]
rs1773062	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1815697	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs1891209	1.00[CEU][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1935220	0.81[EUR][1000 genomes]
rs1935221	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs1935223	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1954220	0.85[EUR][1000 genomes]
rs2094519	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs2094520	1.00[CEU][hapmap];0.89[YRI][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2105313	0.85[EUR][1000 genomes]
rs2105314	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs2149230	0.94[EUR][1000 genomes]
rs2182934	1.00[CEU][hapmap];0.90[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2182935	1.00[CEU][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2769714	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2769716	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2794624	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs2794625	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs2794626	0.85[EUR][1000 genomes]
rs2794627	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs2794628	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs2794629	0.85[EUR][1000 genomes]
rs2794631	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2794638	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2987037	0.85[ASN][1000 genomes]
rs2987040	0.85[ASN][1000 genomes]
rs2987043	0.85[ASN][1000 genomes]
rs2987044	0.85[ASN][1000 genomes]
rs2987045	0.85[EUR][1000 genomes]
rs2987046	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2987048	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2987054	1.00[CEU][hapmap];0.85[YRI][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2987057	1.00[CEU][hapmap];0.85[YRI][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2987058	0.91[EUR][1000 genomes]
rs2987060	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs2987061	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs2987062	0.85[EUR][1000 genomes]
rs2987063	0.92[ASN][1000 genomes]
rs2987065	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2987066	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2987073	0.92[ASN][1000 genomes]
rs2987076	0.92[ASN][1000 genomes]
rs2995024	0.86[EUR][1000 genomes]
rs2995025	0.88[EUR][1000 genomes]
rs3008669	0.92[ASN][1000 genomes]
rs3008680	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3008682	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3008683	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3008685	0.85[EUR][1000 genomes]
rs3008691	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs3008692	0.94[EUR][1000 genomes]
rs3008693	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs3008695	0.94[EUR][1000 genomes]
rs3008698	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs3008700	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3008712	0.85[ASN][1000 genomes]
rs3008737	0.85[ASN][1000 genomes]
rs3124459	0.80[EUR][1000 genomes]
rs3750402	0.92[ASN][1000 genomes]
rs6474978	0.88[EUR][1000 genomes]
rs6474979	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs6474996	0.85[ASN][1000 genomes]
rs7028328	0.84[EUR][1000 genomes]
rs7039881	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs7388793	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs7469281	0.92[ASN][1000 genomes]
rs770190	0.89[EUR][1000 genomes]
rs770192	0.85[EUR][1000 genomes]
rs770193	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs770194	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs770195	0.84[EUR][1000 genomes]
rs770196	1.00[CEU][hapmap]
rs770197	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs770198	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs770199	1.00[CEU][hapmap];0.86[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];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs770204	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs770205	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs770206	1.00[CEU][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs770207	0.87[EUR][1000 genomes]
rs770210	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs770212	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs770214	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs770217	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs770218	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs770219	0.82[EUR][1000 genomes]
rs7860354	0.81[EUR][1000 genomes]
rs7860463	0.85[EUR][1000 genomes]
rs7860856	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7861105	0.94[EUR][1000 genomes]
rs809493	0.88[EUR][1000 genomes]
rs9406546	0.85[EUR][1000 genomes]
rs9407664	0.82[EUR][1000 genomes]
rs9407665	0.84[EUR][1000 genomes]
rs9407668	0.85[EUR][1000 genomes]
rs961116	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 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

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15902000-15914200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:15908800-15909600	Enhancers	HSMMtube	muscle
3	chr9:15908800-15910200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr9:15908800-15910200	Enhancers	HSMM	muscle
5	chr9:15909000-15909600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr9:15909000-15910200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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