Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10195330	0.86[EUR][1000 genomes]
rs10199508	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10203762	0.88[EUR][1000 genomes]
rs10928119	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11885368	0.82[EUR][1000 genomes]
rs11891104	0.83[EUR][1000 genomes]
rs11896157	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12373690	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12373842	0.88[EUR][1000 genomes]
rs12471563	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12613378	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12614785	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12622890	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13386614	0.86[EUR][1000 genomes]
rs13390324	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13400579	0.82[EUR][1000 genomes]
rs13412600	0.82[EUR][1000 genomes]
rs13412704	0.82[EUR][1000 genomes]
rs1437342	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16846899	0.82[EUR][1000 genomes]
rs16846913	0.88[EUR][1000 genomes]
rs2028131	0.82[EUR][1000 genomes]
rs2028133	0.82[EUR][1000 genomes]
rs2164700	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2196599	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2381155	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs28681388	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs355541	0.82[EUR][1000 genomes]
rs56078839	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56261462	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7563507	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv583214	chr2:142299923-142458316	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
2	nsv834394	chr2:142430225-142593264	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr2:142450000-142451000	Bivalent Enhancer	Fetal Heart	heart

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