Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs12334344	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12549153	0.86[EUR][1000 genomes]
rs1588499	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16925109	0.92[EUR][1000 genomes]
rs16925119	0.92[EUR][1000 genomes]
rs2326443	0.84[ASN][1000 genomes]
rs2326444	0.84[ASN][1000 genomes]
rs28590033	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4354297	0.82[ASN][1000 genomes]
rs4629854	0.86[EUR][1000 genomes]
rs4644228	0.92[EUR][1000 genomes]
rs55641496	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56394800	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57114745	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60587092	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62504703	0.92[EUR][1000 genomes]
rs62504733	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62506400	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62506401	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6471803	0.82[ASN][1000 genomes]
rs6471819	0.82[ASN][1000 genomes]
rs6471820	0.82[ASN][1000 genomes]
rs6982408	0.84[ASN][1000 genomes]
rs6984242	0.82[ASN][1000 genomes]
rs6988338	0.84[ASN][1000 genomes]
rs7017889	0.82[ASN][1000 genomes]
rs72655599	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7835908	0.85[ASN][1000 genomes]
rs7836602	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030564	chr8:60445016-60752655	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv539630	chr8:60445016-60752655	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv890942	chr8:60639357-60686330	Enhancers Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	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	chr8:60679800-60680600	Enhancers	Pancreatic Islets	Pancreatic Islet

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