Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs12787057	0.85[ASN][1000 genomes]
rs12788163	0.81[ASN][1000 genomes]
rs12792816	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1368135	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17310982	0.83[AMR][1000 genomes]
rs2015782	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs4944085	0.83[AMR][1000 genomes]
rs4945024	0.83[AMR][1000 genomes]
rs570559	0.85[AMR][1000 genomes]
rs57398723	0.83[AMR][1000 genomes]
rs584046	0.85[AMR][1000 genomes]
rs601293	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs61329757	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61544743	0.80[AMR][1000 genomes]
rs61897970	0.81[ASN][1000 genomes]
rs664133	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs683195	0.83[AMR][1000 genomes]
rs684644	0.83[AMR][1000 genomes]
rs7120248	0.82[AMR][1000 genomes]
rs7127841	0.81[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	esv3381903	chr11:75123498-75587233	Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	81 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	chr11:75410200-75417000	Weak transcription	Fetal Intestine Large	intestine

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