Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10789538	0.97[ASN][1000 genomes]
rs10789539	0.97[ASN][1000 genomes]
rs10890573	0.97[ASN][1000 genomes]
rs10890574	0.95[ASN][1000 genomes]
rs10890575	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11211887	0.91[ASN][1000 genomes]
rs12146527	0.95[ASN][1000 genomes]
rs12293752	0.91[ASN][1000 genomes]
rs1487904	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1487905	0.97[ASN][1000 genomes]
rs1487906	0.97[ASN][1000 genomes]
rs1843988	0.95[ASN][1000 genomes]
rs2171459	0.90[ASN][1000 genomes]
rs3763816	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3763817	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3763818	0.96[ASN][1000 genomes]
rs4121519	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4754166	0.96[ASN][1000 genomes]
rs7482785	0.91[ASN][1000 genomes]
rs7931295	0.96[ASN][1000 genomes]
rs7942149	0.96[ASN][1000 genomes]
rs996782	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	nsv898359	chr11:106523574-106656863	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106552800-106628200	Weak transcription	Pancreas	Pancrea
2	chr11:106607800-106629000	Weak transcription	Fetal Lung	lung
3	chr11:106616600-106617000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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