Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10789540	0.98[ASN][1000 genomes]
rs10890569	0.94[ASN][1000 genomes]
rs11608184	0.94[ASN][1000 genomes]
rs12788085	0.94[ASN][1000 genomes]
rs12798695	0.94[ASN][1000 genomes]
rs12800630	0.94[ASN][1000 genomes]
rs12803679	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1487908	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1565161	0.95[ASN][1000 genomes]
rs1601806	0.94[ASN][1000 genomes]
rs17565192	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17649831	0.94[ASN][1000 genomes]
rs17650551	0.91[ASN][1000 genomes]
rs2220375	0.98[ASN][1000 genomes]
rs3763817	0.83[EUR][1000 genomes]
rs4121677	0.94[ASN][1000 genomes]
rs67740566	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67981963	0.94[ASN][1000 genomes]
rs7103063	0.98[ASN][1000 genomes]
rs7126017	0.91[ASN][1000 genomes]
rs7126092	0.91[ASN][1000 genomes]
rs7129036	0.98[ASN][1000 genomes]
rs7950329	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7950851	0.84[AMR][1000 genomes];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	chr11:106595600-106604800	Weak transcription	Fetal Lung	lung
3	chr11:106603400-106604400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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