Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11135546	0.81[AMR][1000 genomes]
rs11739685	0.81[AMR][1000 genomes]
rs11741372	0.81[AMR][1000 genomes]
rs11742020	0.81[AMR][1000 genomes]
rs11742033	0.81[AMR][1000 genomes]
rs11742228	0.81[AMR][1000 genomes]
rs11951691	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11951743	0.92[ASN][1000 genomes]
rs11958382	1.00[ASN][1000 genomes]
rs11958448	0.85[ASN][1000 genomes]
rs4377726	0.81[AMR][1000 genomes]
rs4461658	0.81[AMR][1000 genomes]
rs73154946	0.81[AMR][1000 genomes]
rs73154947	0.81[AMR][1000 genomes]
rs73154954	0.81[AMR][1000 genomes]
rs73154956	0.81[AMR][1000 genomes]
rs73154957	0.81[AMR][1000 genomes]
rs73154962	0.81[AMR][1000 genomes]
rs73154963	0.81[AMR][1000 genomes]
rs73154965	0.81[AMR][1000 genomes]
rs7703831	0.81[AMR][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	nsv525867	chrX:137580983-138439843	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 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	chrX:137885600-137940200	Weak transcription	K562	blood

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