Variant report

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

rs_ID	r²[population]
rs1050563	1.00[ASN][1000 genomes]
rs11675248	1.00[ASN][1000 genomes]
rs12104956	1.00[ASN][1000 genomes]
rs17625931	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17668045	1.00[ASN][1000 genomes]
rs17668081	1.00[ASN][1000 genomes]
rs17671192	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4668524	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55650814	1.00[ASN][1000 genomes]
rs55688218	1.00[ASN][1000 genomes]
rs55977534	1.00[ASN][1000 genomes]
rs56198546	1.00[ASN][1000 genomes]
rs56329647	1.00[ASN][1000 genomes]
rs62106487	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6713667	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72781796	1.00[ASN][1000 genomes]
rs72781798	1.00[ASN][1000 genomes]
rs72781800	1.00[ASN][1000 genomes]
rs72781802	1.00[ASN][1000 genomes]
rs72783710	1.00[ASN][1000 genomes]
rs72783713	1.00[ASN][1000 genomes]
rs72783719	1.00[ASN][1000 genomes]
rs72783724	1.00[ASN][1000 genomes]
rs72783730	1.00[ASN][1000 genomes]
rs72783732	1.00[ASN][1000 genomes]
rs72783735	1.00[ASN][1000 genomes]
rs921619	1.00[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	nsv915888	chr2:7197783-7461967	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer 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	chr2:7302600-7303600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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