Variant report

Variant	rs73601364
Chromosome Location	chr8:54125832-54125833
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs16918832	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16918875	1.00[EUR][1000 genomes]
rs16918900	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16918955	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34418807	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57537478	1.00[EUR][1000 genomes]
rs57796760	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58121794	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58534275	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58861077	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60521056	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60721705	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61410012	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6988508	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6996658	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7016275	1.00[EUR][1000 genomes]
rs73585649	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73585658	1.00[EUR][1000 genomes]
rs73589347	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73589385	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73601368	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73602836	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73602840	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73602841	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73602844	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73602860	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73679682	1.00[EUR][1000 genomes]
rs7816233	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7822011	1.00[EUR][1000 genomes]
rs7822111	1.00[EUR][1000 genomes]
rs7829470	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7832039	0.93[EUR][1000 genomes]
rs7839445	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	nsv1016224	chr8:53719941-54367534	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv530534	chr8:53787984-54367353	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3377304	chr8:53873441-54380875	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv611375	chr8:54122620-54130075	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	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	chr8:54125200-54126800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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