Variant report

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

rs_ID	r²[population]
rs11706756	0.81[ASN][1000 genomes]
rs17005397	0.87[ASN][1000 genomes]
rs34550101	0.87[ASN][1000 genomes]
rs4525874	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4855355	0.87[ASN][1000 genomes]
rs4855548	0.83[ASN][1000 genomes]
rs4855549	0.84[ASN][1000 genomes]
rs4855550	0.85[ASN][1000 genomes]
rs55978846	0.87[ASN][1000 genomes]
rs58798960	0.87[ASN][1000 genomes]
rs60204248	0.87[ASN][1000 genomes]
rs61207882	0.87[ASN][1000 genomes]
rs6762052	0.84[ASN][1000 genomes]
rs6767493	0.84[ASN][1000 genomes]
rs6778830	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6779171	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6806271	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6808756	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7613159	0.81[ASN][1000 genomes]
rs7638997	0.83[ASN][1000 genomes]
rs881804	0.83[ASN][1000 genomes]
rs937863	0.83[ASN][1000 genomes]
rs9815992	0.82[ASN][1000 genomes]
rs9825485	0.84[ASN][1000 genomes]
rs9843043	0.84[ASN][1000 genomes]
rs9853232	1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9864756	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	nsv876933	chr3:69059023-69227379	Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 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	chr3:69204800-69205400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood

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