Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12666343	0.84[ASN][1000 genomes]
rs13238059	1.00[ASN][1000 genomes]
rs13242525	1.00[ASN][1000 genomes]
rs13244158	0.86[ASN][1000 genomes]
rs2864463	1.00[ASN][1000 genomes]
rs2902759	1.00[ASN][1000 genomes]
rs2902836	1.00[ASN][1000 genomes]
rs34752925	0.81[ASN][1000 genomes]
rs35227483	0.88[ASN][1000 genomes]
rs35712623	0.86[ASN][1000 genomes]
rs35746743	0.95[ASN][1000 genomes]
rs35850158	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3846975	1.00[ASN][1000 genomes]
rs4718638	1.00[ASN][1000 genomes]
rs4718641	1.00[ASN][1000 genomes]
rs62458311	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62458316	1.00[ASN][1000 genomes]
rs6946477	1.00[ASN][1000 genomes]
rs6951285	1.00[ASN][1000 genomes]
rs6955469	1.00[ASN][1000 genomes]
rs6955571	1.00[ASN][1000 genomes]
rs6973904	1.00[ASN][1000 genomes]
rs6975069	1.00[ASN][1000 genomes]
rs71535653	1.00[ASN][1000 genomes]
rs71535654	1.00[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	nsv1027532	chr7:67261526-67387398	Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3416894	chr7:67314017-67315915	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:67314400-67315600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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