Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10510529	0.91[CHB][hapmap];0.82[CHD][hapmap];0.90[GIH][hapmap];0.93[MEX][hapmap]
rs10510530	0.88[CEU][hapmap]
rs11129066	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs11129067	0.92[CHD][hapmap];0.92[JPT][hapmap]
rs11709549	0.83[ASN][1000 genomes]
rs11710808	0.91[CHD][hapmap];0.92[JPT][hapmap]
rs11711745	0.94[CEU][hapmap];0.82[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11716879	0.89[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs12639237	0.88[CEU][hapmap]
rs7614013	0.84[CEU][hapmap];0.90[CHB][hapmap];0.92[JPT][hapmap]
rs7616332	0.81[CEU][hapmap];0.89[CHB][hapmap];0.92[JPT][hapmap]
rs7616503	0.83[CHB][hapmap];0.92[JPT][hapmap]
rs7619731	0.92[CHD][hapmap];0.92[JPT][hapmap]
rs7624127	0.83[CEU][hapmap];0.83[CHB][hapmap];0.92[JPT][hapmap]
rs9811913	1.00[JPT][hapmap]
rs9844836	0.84[ASN][1000 genomes]
rs9844916	0.88[CHD][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs9845451	0.84[ASN][1000 genomes]
rs9845488	0.82[ASN][1000 genomes]
rs9852024	0.83[CEU][hapmap];0.82[JPT][hapmap]
rs9861611	0.89[CEU][hapmap];0.91[CHB][hapmap];0.91[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.82[TSI][hapmap];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9862793	0.88[CEU][hapmap]
rs9875182	0.88[CEU][hapmap]
rs9876850	0.84[ASN][1000 genomes]
rs9882628	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

Chromatin state (count:0 , 50 per page) page:

No data

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