Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10225537	1.00[AMR][1000 genomes]
rs10242118	1.00[AMR][1000 genomes]
rs10249690	1.00[EUR][1000 genomes]
rs10251214	1.00[AMR][1000 genomes]
rs10264392	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10268111	1.00[EUR][1000 genomes]
rs10270262	1.00[AMR][1000 genomes]
rs17156077	1.00[AMR][1000 genomes]
rs28534983	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28576424	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28584565	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28690916	1.00[AMR][1000 genomes]
rs55645791	1.00[AMR][1000 genomes]
rs56231121	1.00[AMR][1000 genomes]
rs56892213	1.00[AMR][1000 genomes]
rs57881876	1.00[AMR][1000 genomes]
rs60796314	1.00[AMR][1000 genomes]
rs6971377	1.00[AMR][1000 genomes]
rs6979246	1.00[AMR][1000 genomes]
rs73713177	1.00[AMR][1000 genomes]
rs73713178	1.00[AMR][1000 genomes]
rs73713180	1.00[AMR][1000 genomes]
rs73713181	1.00[AMR][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	nsv817371	chr7:108199882-108649799	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 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	chr7:108295800-108300400	Weak transcription	Liver	Liver

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