Variant report

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

rs_ID	r²[population]
rs1324872	1.00[AMR][1000 genomes]
rs1328045	1.00[AMR][1000 genomes]
rs1571322	1.00[AMR][1000 genomes]
rs1755463	1.00[AFR][1000 genomes]
rs1853721	1.00[AMR][1000 genomes]
rs1856995	1.00[AMR][1000 genomes]
rs2988041	1.00[AFR][1000 genomes]
rs2988043	1.00[AFR][1000 genomes]
rs2988047	1.00[AFR][1000 genomes]
rs2991462	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2991508	1.00[EUR][1000 genomes]
rs4052508	1.00[AMR][1000 genomes]
rs4300513	1.00[AMR][1000 genomes]
rs4885630	1.00[AMR][1000 genomes]
rs588755	1.00[AFR][1000 genomes]
rs592096	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs597726	1.00[AFR][1000 genomes]
rs645414	1.00[EUR][1000 genomes]
rs6563092	1.00[AMR][1000 genomes]
rs662380	1.00[AFR][1000 genomes]
rs674280	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs676238	1.00[EUR][1000 genomes]
rs680178	1.00[AFR][1000 genomes]
rs686483	1.00[EUR][1000 genomes]
rs7324585	1.00[AMR][1000 genomes]
rs7334029	1.00[AMR][1000 genomes]
rs7993115	1.00[AMR][1000 genomes]
rs927696	1.00[AMR][1000 genomes]
rs9545056	1.00[AMR][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	nsv916612	chr13:79669876-79820692	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1045334	chr13:79671094-79809717	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1046915	chr13:79695827-79756956	Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:79700400-79702800	Enhancers	HMEC	breast
2	chr13:79702200-79702600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr13:79702200-79702600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr13:79702200-79702800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr13:79702200-79702800	Enhancers	NHEK	skin

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