Variant report

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

rs_ID	r²[population]
rs11004028	0.82[ASN][1000 genomes]
rs11004029	0.82[ASN][1000 genomes]
rs11004030	0.82[ASN][1000 genomes]
rs11004031	0.82[ASN][1000 genomes]
rs11004032	0.82[ASN][1000 genomes]
rs11594112	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11594638	0.82[ASN][1000 genomes]
rs11597275	0.82[AMR][1000 genomes]
rs11598843	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12243005	0.82[ASN][1000 genomes]
rs12244555	0.82[ASN][1000 genomes]
rs12244759	0.82[ASN][1000 genomes]
rs12250607	0.82[ASN][1000 genomes]
rs12250681	0.82[ASN][1000 genomes]
rs12251985	0.82[ASN][1000 genomes]
rs12252125	0.82[ASN][1000 genomes]
rs12252197	0.82[ASN][1000 genomes]
rs12253866	0.82[ASN][1000 genomes]
rs12257312	0.82[ASN][1000 genomes]
rs12257494	0.82[ASN][1000 genomes]
rs1911379	0.82[ASN][1000 genomes]
rs28701623	0.82[ASN][1000 genomes]
rs3812657	0.82[ASN][1000 genomes]
rs72794984	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949692	chr10:55502542-55893206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv869303	chr10:55714219-55857931	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No data

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