Variant report

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

rs_ID	r²[population]
rs10265603	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10281056	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10954161	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11761076	0.82[AFR][1000 genomes]
rs11761988	0.91[ASN][1000 genomes]
rs11764631	0.89[ASN][1000 genomes]
rs11767380	0.91[ASN][1000 genomes]
rs1419429	0.82[AFR][1000 genomes]
rs1419430	0.91[ASN][1000 genomes]
rs1557643	0.91[ASN][1000 genomes]
rs17715255	0.91[ASN][1000 genomes]
rs17715285	0.91[ASN][1000 genomes]
rs35195581	0.91[ASN][1000 genomes]
rs4551267	0.83[ASN][1000 genomes]
rs4728072	0.91[ASN][1000 genomes]
rs4728073	0.91[ASN][1000 genomes]
rs4728075	0.88[ASN][1000 genomes]
rs4731370	0.91[ASN][1000 genomes]
rs55657491	0.91[ASN][1000 genomes]
rs57867532	0.89[ASN][1000 genomes]
rs58894662	0.91[ASN][1000 genomes]
rs6970053	0.91[ASN][1000 genomes]
rs6976685	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs990032	0.91[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	nsv831122	chr7:127143207-127357885	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	esv1801682	chr7:127188972-127209982	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127186600-127200400	Weak transcription	Pancreas	Pancrea

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