Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10236653	0.80[CEU][hapmap]
rs10499442	0.86[CEU][hapmap]
rs11767890	0.81[CEU][hapmap]
rs11980816	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs12669548	0.88[CEU][hapmap]
rs12674261	0.85[CEU][hapmap]
rs12699622	0.85[CEU][hapmap]
rs1431521	0.86[CEU][hapmap]
rs1431528	0.88[CEU][hapmap]
rs1560576	0.84[CEU][hapmap];0.83[CHB][hapmap]
rs182034	0.96[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1835675	0.84[EUR][1000 genomes]
rs1897300	0.89[CEU][hapmap]
rs196751	0.88[CEU][hapmap];0.82[EUR][1000 genomes]
rs196757	0.82[CEU][hapmap]
rs1991685	0.85[CEU][hapmap]
rs3823843	0.85[CEU][hapmap]
rs4370419	0.86[CEU][hapmap]
rs6461104	0.85[CEU][hapmap]
rs7807072	0.85[CEU][hapmap]
rs987448	0.89[CEU][hapmap]
rs987449	0.85[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv915603	chr7:14443884-14624268	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv1848567	chr7:14464118-14579801	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv887707	chr7:14471682-14576163	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No data

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