Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10517184	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs10517185	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs10938482	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs11733050	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs11945405	0.86[JPT][hapmap]
rs12331254	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs13107066	1.00[CHB][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs17461863	1.00[JPT][hapmap]
rs17600442	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs17600511	0.82[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap]
rs17653449	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs4289418	0.86[JPT][hapmap]
rs4336201	0.86[JPT][hapmap]
rs4694846	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs4695220	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs6447550	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs6814130	0.86[JPT][hapmap]
rs6817416	0.86[JPT][hapmap]
rs6830892	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs7439087	0.86[JPT][hapmap]
rs7677890	0.82[CHB][hapmap];1.00[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	nsv998919	chr4:47207023-47476876	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No data

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