Variant report

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1018991	0.83[CHB][hapmap];0.88[CHD][hapmap]
rs10265626	0.81[CHB][hapmap]
rs10267232	0.83[CHB][hapmap];0.82[CHD][hapmap]
rs10487689	1.00[CEU][hapmap];0.81[CHB][hapmap];0.82[CHD][hapmap];1.00[GIH][hapmap];0.81[JPT][hapmap];0.83[MEX][hapmap];1.00[TSI][hapmap]
rs1304809	0.86[JPT][hapmap];0.81[AFR][1000 genomes]
rs13230403	0.87[CHB][hapmap];0.88[CHD][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs1585815	0.86[JPT][hapmap]
rs2697452	0.85[JPT][hapmap]
rs2697457	0.86[JPT][hapmap]
rs28430910	0.84[ASN][1000 genomes]
rs6464815	0.94[CHB][hapmap];0.88[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs6973129	0.80[CHB][hapmap]
rs700293	0.86[JPT][hapmap]
rs700296	0.81[JPT][hapmap]
rs700311	0.86[JPT][hapmap]
rs7778880	1.00[CHB][hapmap];0.88[CHD][hapmap];0.91[JPT][hapmap]
rs7779464	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs7780096	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs7796301	0.85[CHD][hapmap]
rs826645	0.86[JPT][hapmap]
rs826656	0.86[JPT][hapmap]
rs826657	0.86[JPT][hapmap]
rs826658	0.86[JPT][hapmap]
rs826659	0.85[JPT][hapmap]
rs826660	0.86[JPT][hapmap]
rs826661	0.85[JPT][hapmap]
rs826786	0.85[JPT][hapmap]
rs826812	0.86[JPT][hapmap]
rs826823	0.84[GIH][hapmap];0.86[JPT][hapmap]
rs872713	0.86[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No data

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