Variant report

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

rs_ID	r²[population]
rs10501036	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11029121	0.85[EUR][1000 genomes]
rs1387490	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17242984	0.91[EUR][1000 genomes]
rs17242991	0.91[EUR][1000 genomes]
rs17243005	0.81[EUR][1000 genomes]
rs17243026	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17308726	0.91[EUR][1000 genomes]
rs17308754	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17308761	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17308782	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56099303	0.88[EUR][1000 genomes]
rs56175671	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56288222	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs66470744	0.91[EUR][1000 genomes]
rs67802819	0.91[EUR][1000 genomes]
rs72885785	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72885787	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72887618	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72887620	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72887634	0.89[AMR][1000 genomes];0.90[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	esv2760599	chr11:25186984-26159450	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr11:26117600-26120000	Enhancers	Fetal Lung	lung

Quick Search: