Variant report

Variant	rs34776422
Chromosome Location	chr2:212605856-212605857
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10205612	0.91[ASN][1000 genomes]
rs10432443	0.89[ASN][1000 genomes]
rs10432444	0.89[ASN][1000 genomes]
rs10432445	0.89[ASN][1000 genomes]
rs10432526	0.84[ASN][1000 genomes]
rs10432527	0.89[ASN][1000 genomes]
rs10932396	0.89[ASN][1000 genomes]
rs10932397	0.89[ASN][1000 genomes]
rs10932398	0.90[ASN][1000 genomes]
rs10932400	0.90[ASN][1000 genomes]
rs11685063	0.91[ASN][1000 genomes]
rs11685867	0.90[ASN][1000 genomes]
rs11690747	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12052854	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12052855	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12987993	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13003936	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13004180	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13004391	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13004899	0.83[ASN][1000 genomes]
rs13008293	0.89[ASN][1000 genomes]
rs13010892	0.99[ASN][1000 genomes]
rs13013901	0.89[ASN][1000 genomes]
rs13020626	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13023789	0.90[ASN][1000 genomes]
rs13024502	0.89[ASN][1000 genomes]
rs13025061	0.81[EUR][1000 genomes]
rs13025068	0.97[ASN][1000 genomes]
rs13025192	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13030400	0.92[ASN][1000 genomes]
rs13030927	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13032058	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13032070	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34040017	0.91[ASN][1000 genomes]
rs34156641	0.94[ASN][1000 genomes]
rs34269326	0.97[ASN][1000 genomes]
rs34937662	0.97[ASN][1000 genomes]
rs35419573	0.89[ASN][1000 genomes]
rs35623699	0.89[ASN][1000 genomes]
rs35720933	0.89[ASN][1000 genomes]
rs35726292	0.89[ASN][1000 genomes]
rs35761042	0.83[ASN][1000 genomes]
rs35870876	0.89[ASN][1000 genomes]
rs36045110	0.89[ASN][1000 genomes]
rs56017633	0.89[ASN][1000 genomes]
rs57367594	0.89[ASN][1000 genomes]
rs6435665	0.97[ASN][1000 genomes]
rs6435666	0.90[ASN][1000 genomes]
rs6435668	0.89[ASN][1000 genomes]
rs6435669	0.89[ASN][1000 genomes]
rs6707801	0.90[ASN][1000 genomes]
rs6722322	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6722576	0.89[ASN][1000 genomes]
rs6722824	0.84[ASN][1000 genomes]
rs6731471	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6733063	0.89[ASN][1000 genomes]
rs6733070	0.87[ASN][1000 genomes]
rs6738017	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6738219	0.97[ASN][1000 genomes]
rs6749096	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6757068	0.91[ASN][1000 genomes]
rs67838351	0.89[ASN][1000 genomes]
rs71422755	0.99[ASN][1000 genomes]
rs7419259	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7422996	0.89[ASN][1000 genomes]
rs7558449	0.90[ASN][1000 genomes]
rs7558651	0.89[ASN][1000 genomes]
rs7572424	0.88[ASN][1000 genomes]
rs7573116	0.89[ASN][1000 genomes]
rs7582099	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7593713	0.97[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	esv34128	chr2:212581485-212857122	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 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	chr2:212602400-212606200	Weak transcription	Fetal Heart	heart

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