Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11158459	0.90[CHB][hapmap]
rs11623063	0.82[CHB][hapmap]
rs11625796	0.82[CHB][hapmap]
rs12431704	0.82[CHB][hapmap]
rs12431729	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12433909	0.92[CEU][hapmap]
rs12883703	1.00[CEU][hapmap];0.81[JPT][hapmap]
rs1980561	1.00[CEU][hapmap];0.81[JPT][hapmap]
rs243146	0.88[CEU][hapmap]
rs243149	0.88[CEU][hapmap];0.86[CHB][hapmap]
rs243155	0.88[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap]
rs243156	0.88[CEU][hapmap];1.00[CHB][hapmap]
rs243157	0.88[CEU][hapmap];1.00[CHB][hapmap]
rs243159	0.88[CEU][hapmap]
rs243162	0.88[CEU][hapmap]
rs34487983	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4146434	0.82[CHB][hapmap]
rs4146435	0.83[CHB][hapmap]
rs71414475	0.82[EUR][1000 genomes]
rs7155227	0.83[CHB][hapmap]
rs7155426	0.87[CEU][hapmap];0.81[JPT][hapmap]
rs7155469	0.82[CHB][hapmap]
rs7156354	0.81[CHB][hapmap]
rs9972116	0.82[CHB][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	nsv1042953	chr14:63314591-63384260	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No data

Quick Search:

Input of quick search could be: