Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12666343	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12698625	0.86[ASN][1000 genomes]
rs13238059	0.86[ASN][1000 genomes]
rs13242525	0.86[ASN][1000 genomes]
rs13244158	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2864463	0.86[ASN][1000 genomes]
rs2902759	0.86[ASN][1000 genomes]
rs2902836	0.86[ASN][1000 genomes]
rs34752925	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35227483	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35746743	0.86[ASN][1000 genomes]
rs35850158	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3846975	0.86[ASN][1000 genomes]
rs4718638	0.86[ASN][1000 genomes]
rs4718641	0.86[ASN][1000 genomes]
rs62458311	0.86[ASN][1000 genomes]
rs62458316	0.86[ASN][1000 genomes]
rs6946477	0.86[ASN][1000 genomes]
rs6951285	0.86[ASN][1000 genomes]
rs6955469	0.86[ASN][1000 genomes]
rs6955571	0.86[ASN][1000 genomes]
rs6973904	0.86[ASN][1000 genomes]
rs6975069	0.86[ASN][1000 genomes]
rs71535653	0.86[ASN][1000 genomes]
rs71535654	0.86[ASN][1000 genomes]
rs9647903	0.84[EUR][1000 genomes]
rs9647904	0.82[EUR][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	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:67311200-67313200	Enhancers	Brain Germinal Matrix	brain

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