Variant report

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

rs_ID	r²[population]
rs11994968	1.00[EUR][1000 genomes]
rs1400551	1.00[EUR][1000 genomes]
rs16934389	1.00[EUR][1000 genomes]
rs16934407	1.00[EUR][1000 genomes]
rs16934575	1.00[EUR][1000 genomes]
rs16934578	1.00[EUR][1000 genomes]
rs57801041	1.00[EUR][1000 genomes]
rs58125593	1.00[EUR][1000 genomes]
rs6981953	1.00[EUR][1000 genomes]
rs6982194	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6998686	1.00[EUR][1000 genomes]
rs6999119	1.00[EUR][1000 genomes]
rs72664912	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72664937	1.00[EUR][1000 genomes]
rs72664939	1.00[EUR][1000 genomes]
rs72664940	1.00[EUR][1000 genomes]
rs72664943	1.00[EUR][1000 genomes]
rs72664944	1.00[EUR][1000 genomes]
rs73262970	1.00[EUR][1000 genomes]
rs73683565	1.00[EUR][1000 genomes]
rs73683567	1.00[EUR][1000 genomes]
rs7827049	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028889	chr8:69026806-69308725	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv948687	chr8:69041121-69642540	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1031040	chr8:69265471-69315554	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv508512	chr8:69268794-69324532	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69290800-69295600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr8:69292200-69295800	Weak transcription	Aorta	Aorta

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