Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11129054	0.84[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap]
rs12107907	0.84[CEU][hapmap];0.83[CHB][hapmap]
rs13079500	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13100427	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1389664	0.91[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1494225	0.95[CHD][hapmap];0.91[JPT][hapmap]
rs1603022	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1603023	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap]
rs1966824	0.84[ASW][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap]
rs35821736	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3749374	0.83[GIH][hapmap]
rs3762776	0.83[GIH][hapmap]
rs4597736	0.88[AMR][1000 genomes]
rs4858401	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs4858402	0.88[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap];0.95[MEX][hapmap];0.96[TSI][hapmap]
rs6778816	0.87[CHB][hapmap];0.91[JPT][hapmap]
rs903289	0.88[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs935736	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs982355	0.95[CHB][hapmap];0.98[CHD][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs9863827	0.82[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003211	chr3:22244883-22584229	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv536520	chr3:22244883-22584229	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv428082	chr3:22397625-22539817	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv834634	chr3:22420053-22574021	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv526662	chr3:22426918-22441261	Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:22440800-22442000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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