Variant report

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

rs_ID	r²[population]
rs10483639	0.93[EUR][1000 genomes]
rs12587434	0.90[EUR][1000 genomes]
rs12589758	0.90[EUR][1000 genomes]
rs17127992	0.99[EUR][1000 genomes]
rs17128004	0.93[EUR][1000 genomes]
rs2057368	0.91[EUR][1000 genomes]
rs2057369	0.92[EUR][1000 genomes]
rs2878168	0.93[EUR][1000 genomes]
rs2878170	0.84[ASN][1000 genomes]
rs4411417	0.93[EUR][1000 genomes]
rs55985131	0.86[EUR][1000 genomes]
rs57875940	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58992937	0.82[ASN][1000 genomes]
rs59750960	0.81[ASN][1000 genomes]
rs60851395	0.81[ASN][1000 genomes]
rs7147737	0.83[EUR][1000 genomes]
rs7148266	0.92[EUR][1000 genomes]
rs7151058	0.98[EUR][1000 genomes]
rs7154323	0.92[EUR][1000 genomes]
rs7155309	0.88[EUR][1000 genomes]
rs72713453	0.98[EUR][1000 genomes]
rs72713456	0.98[EUR][1000 genomes]
rs72713467	0.93[EUR][1000 genomes]
rs72713477	1.00[AFR][1000 genomes]
rs752688	0.93[EUR][1000 genomes]
rs841	0.92[EUR][1000 genomes]
rs9671455	0.90[EUR][1000 genomes]
rs9671850	0.88[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	nsv530042	chr14:55208170-55386966	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 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	chr14:55293800-55306400	Weak transcription	Aorta	Aorta

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