Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11690747	0.81[ASN][1000 genomes]
rs13010892	0.84[ASN][1000 genomes]
rs13020626	0.83[ASN][1000 genomes]
rs13030667	0.86[CHB][hapmap];0.91[ASN][1000 genomes]
rs34269326	0.81[ASN][1000 genomes]
rs34776422	0.83[ASN][1000 genomes]
rs34937662	0.81[ASN][1000 genomes]
rs35761042	0.98[ASN][1000 genomes]
rs6435665	0.81[ASN][1000 genomes]
rs6706010	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs6706030	0.87[CHB][hapmap];0.91[ASN][1000 genomes]
rs6711487	0.82[CHB][hapmap]
rs6722322	0.95[YRI][hapmap];0.82[ASN][1000 genomes]
rs6722824	0.85[CHB][hapmap];0.87[YRI][hapmap];0.98[ASN][1000 genomes]
rs6738219	0.81[ASN][1000 genomes]
rs6746063	0.83[EUR][1000 genomes]
rs71422755	0.82[ASN][1000 genomes]
rs7588792	0.84[CEU][hapmap];0.83[EUR][1000 genomes]
rs7593713	0.81[ASN][1000 genomes]
rs7597007	0.87[CHB][hapmap]
rs7605314	0.82[CHB][hapmap]

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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