Variant report

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

rs_ID	r²[population]
rs11563782	0.82[CEU][hapmap]
rs17644601	0.82[CEU][hapmap]
rs17862293	0.82[CEU][hapmap];0.85[ASN][1000 genomes]
rs17862309	1.00[CEU][hapmap]
rs17862310	0.85[CEU][hapmap]
rs17862320	0.82[CEU][hapmap]
rs17863211	0.82[CEU][hapmap]
rs17863237	1.00[CEU][hapmap]
rs17863242	0.85[CEU][hapmap]
rs17864127	0.82[CEU][hapmap]
rs17864153	1.00[CEU][hapmap]
rs17864154	1.00[CEU][hapmap]
rs17864156	1.00[CEU][hapmap]
rs17864160	0.85[CEU][hapmap]
rs17867759	0.82[CEU][hapmap]
rs17867764	0.82[CEU][hapmap];0.81[ASN][1000 genomes]
rs17867770	0.82[CEU][hapmap]
rs17867775	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17869212	0.82[CEU][hapmap]
rs2237793	0.82[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889189	chr7:126699088-126963028	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2761367	chr7:126717157-126865324	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1027369	chr7:126772111-126798871	Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No data

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