Variant report

Variant	rs62183023
Chromosome Location	chr2:212618746-212618747
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12622176	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35444377	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4130781	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4130782	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4132462	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55758468	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55769536	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55897719	0.84[EUR][1000 genomes]
rs56405287	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61079605	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62182986	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62182989	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62182991	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62182999	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62183021	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62183024	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62183028	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62183029	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62183031	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62183034	0.82[ASN][1000 genomes]
rs6749448	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72946582	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72948506	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7422793	0.82[EUR][1000 genomes]
rs7556896	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7600261	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7601502	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[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:2 , 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
2	chr2:212617000-212620800	Weak transcription	Fetal Lung	lung

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