Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs4351181	0.81[AFR][1000 genomes]
rs4485908	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4565246	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60047729	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60899707	1.00[AMR][1000 genomes]
rs6885172	1.00[EUR][1000 genomes]
rs73129459	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73129482	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73129483	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73131509	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73131513	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73131588	0.81[AFR][1000 genomes]
rs73131595	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73133057	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73133062	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73133075	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73133077	1.00[AMR][1000 genomes]
rs73133079	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73134921	1.00[AMR][1000 genomes]
rs73134929	1.00[AMR][1000 genomes]
rs73134939	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	nsv882378	chr5:91477046-91601492	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr5:91558400-91558600	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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