Variant report

Variant	rs13025061
Chromosome Location	chr2:212611566-212611567
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10432443	0.82[ASN][1000 genomes]
rs10432444	0.82[ASN][1000 genomes]
rs10432445	0.82[ASN][1000 genomes]
rs10432527	0.82[ASN][1000 genomes]
rs10932396	0.81[ASN][1000 genomes]
rs10932397	0.81[ASN][1000 genomes]
rs10932398	0.82[ASN][1000 genomes]
rs10932400	0.82[ASN][1000 genomes]
rs11685063	0.83[ASN][1000 genomes]
rs11685867	0.82[ASN][1000 genomes]
rs11690747	0.82[EUR][1000 genomes]
rs12052854	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12052855	0.85[ASN][1000 genomes]
rs12987993	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13003936	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13004180	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13004391	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13008293	0.81[ASN][1000 genomes]
rs13013901	0.82[ASN][1000 genomes]
rs13020626	0.80[EUR][1000 genomes]
rs13023789	0.83[ASN][1000 genomes]
rs13024502	0.82[ASN][1000 genomes]
rs13025192	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13030400	0.84[ASN][1000 genomes]
rs13030927	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13032058	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13032070	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34040017	0.83[ASN][1000 genomes]
rs34156641	0.81[ASN][1000 genomes]
rs34776422	0.81[EUR][1000 genomes]
rs35419573	0.82[ASN][1000 genomes]
rs35623699	0.82[ASN][1000 genomes]
rs35720933	0.82[ASN][1000 genomes]
rs35726292	0.82[ASN][1000 genomes]
rs35870876	0.81[ASN][1000 genomes]
rs36045110	0.82[ASN][1000 genomes]
rs56017633	0.82[ASN][1000 genomes]
rs57367594	0.82[ASN][1000 genomes]
rs6435666	0.83[ASN][1000 genomes]
rs6435668	0.82[ASN][1000 genomes]
rs6435669	0.82[ASN][1000 genomes]
rs6707801	0.82[ASN][1000 genomes]
rs6722322	0.81[EUR][1000 genomes]
rs6722576	0.82[ASN][1000 genomes]
rs6731471	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6733063	0.82[ASN][1000 genomes]
rs6738017	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6749096	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6757068	0.83[ASN][1000 genomes]
rs67838351	0.82[ASN][1000 genomes]
rs7419259	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7422996	0.82[ASN][1000 genomes]
rs7558449	0.82[ASN][1000 genomes]
rs7558651	0.81[ASN][1000 genomes]
rs7572424	0.80[ASN][1000 genomes]
rs7573116	0.81[ASN][1000 genomes]
rs7582099	0.82[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	chr2:212610200-212626600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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