Variant report

Variant	rs56361294
Chromosome Location	chr7:79650156-79650157
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10231925	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10237290	0.83[AMR][1000 genomes]
rs10237415	0.83[AMR][1000 genomes]
rs10238912	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10242482	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10247323	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10260857	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11974166	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11977309	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11977332	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs12333681	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs28630699	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs34872162	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs35802637	0.95[AFR][1000 genomes]
rs55687904	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56330158	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56761500	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57082352	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57137296	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57291254	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs58876952	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs59312847	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs61390031	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs61586173	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73374533	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73374541	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73374589	0.87[AFR][1000 genomes]
rs73374591	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73376508	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73376538	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73376541	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73376565	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73378605	1.00[AMR][1000 genomes]
rs73708417	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73708491	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73708493	0.85[AFR][1000 genomes];1.00[AMR][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	nsv429785	chr7:79589749-80177049	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv607676	chr7:79636682-79687844	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv818527	chr7:79636682-79687844	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv607677	chr7:79636682-79693050	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79649800-79650400	Enhancers	HepG2	liver

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