Variant report

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

rs_ID	r²[population]
rs11746987	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13174932	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs191162	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs318022	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs318040	0.88[EUR][1000 genomes]
rs318042	0.88[EUR][1000 genomes]
rs318043	0.87[EUR][1000 genomes]
rs318044	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs318045	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs318046	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs318047	0.96[EUR][1000 genomes]
rs318050	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs318051	0.81[AMR][1000 genomes]
rs35350798	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3851439	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3907521	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3913721	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4245981	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4346812	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4957155	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[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	nsv1028390	chr5:41537220-41561373	Weak transcription Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41540200-41541200	Weak transcription	Fetal Heart	heart

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