Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11699698	0.84[ASN][1000 genomes]
rs12481593	0.81[EUR][1000 genomes]
rs12624812	0.81[EUR][1000 genomes]
rs169231	0.82[ASN][1000 genomes]
rs169232	0.95[ASN][1000 genomes]
rs17753094	0.82[ASN][1000 genomes]
rs191830	0.84[ASN][1000 genomes]
rs199812	0.82[ASN][1000 genomes]
rs199813	0.80[ASN][1000 genomes]
rs407847	0.81[ASN][1000 genomes]
rs4393808	0.84[ASN][1000 genomes]
rs4815109	0.82[ASN][1000 genomes]
rs4815110	0.82[ASN][1000 genomes]
rs6137606	0.84[ASN][1000 genomes]
rs6137608	0.84[ASN][1000 genomes]
rs6137609	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6137610	0.82[ASN][1000 genomes]
rs6137611	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6137615	0.81[EUR][1000 genomes]
rs6137616	0.81[EUR][1000 genomes]
rs7263317	0.84[ASN][1000 genomes]
rs7263509	0.84[ASN][1000 genomes]
rs7267431	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7271129	0.84[ASN][1000 genomes]
rs7271196	0.84[ASN][1000 genomes]
rs927170	0.84[ASN][1000 genomes]

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	nsv833942	chr20:22283122-22440749	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:22310400-22314800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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