Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11727424	1.00[ASN][1000 genomes]
rs1355111	1.00[ASN][1000 genomes]
rs167506	1.00[ASN][1000 genomes]
rs313103	1.00[ASN][1000 genomes]
rs313130	1.00[ASN][1000 genomes]
rs313131	1.00[ASN][1000 genomes]
rs313134	1.00[ASN][1000 genomes]
rs313137	1.00[ASN][1000 genomes]
rs313138	1.00[ASN][1000 genomes]
rs432446	1.00[ASN][1000 genomes]
rs4410545	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4440236	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4444841	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4456972	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs60133914	1.00[ASN][1000 genomes]
rs62321712	1.00[ASN][1000 genomes]
rs62321713	1.00[ASN][1000 genomes]
rs62321714	1.00[ASN][1000 genomes]
rs62321715	1.00[ASN][1000 genomes]
rs62321722	1.00[ASN][1000 genomes]
rs62321723	1.00[ASN][1000 genomes]
rs62322676	1.00[ASN][1000 genomes]
rs62322678	1.00[ASN][1000 genomes]
rs62322679	1.00[ASN][1000 genomes]
rs62322680	1.00[ASN][1000 genomes]
rs62322683	1.00[ASN][1000 genomes]
rs62322684	1.00[ASN][1000 genomes]
rs62324762	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	nsv595385	chr4:127383473-127451806	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	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	chr4:127416400-127416800	Flanking Active TSS	K562	blood

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