Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10108963	1.00[CEU][hapmap];0.83[CHB][hapmap]
rs1055168	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[EUR][1000 genomes]
rs10955661	0.81[ASN][1000 genomes]
rs11786953	0.86[EUR][1000 genomes]
rs1478679	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1513520	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1513527	0.84[EUR][1000 genomes]
rs16884700	0.82[JPT][hapmap]
rs1949225	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2279160	1.00[CEU][hapmap];0.87[CHB][hapmap];0.84[EUR][1000 genomes]
rs2927867	0.96[CHB][hapmap];1.00[JPT][hapmap]
rs2927875	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2942849	1.00[CEU][hapmap];0.87[CHB][hapmap];0.85[EUR][1000 genomes]
rs2942850	1.00[CEU][hapmap];0.87[CHB][hapmap];0.85[EUR][1000 genomes]
rs2942854	0.88[EUR][1000 genomes]
rs2954885	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2954900	1.00[CEU][hapmap];0.83[CHB][hapmap];0.85[EUR][1000 genomes]
rs6469456	0.92[CEU][hapmap];0.87[CHB][hapmap];0.81[EUR][1000 genomes]
rs6982808	1.00[CEU][hapmap];0.83[CHB][hapmap]
rs6993017	0.96[CEU][hapmap]
rs7828293	0.92[CEU][hapmap];0.87[CHB][hapmap]
rs7831926	1.00[CEU][hapmap];0.83[CHB][hapmap]
rs899299	0.82[EUR][1000 genomes]
rs922467	1.00[CEU][hapmap];0.87[CHB][hapmap];0.85[EUR][1000 genomes]
rs938248	1.00[CEU][hapmap];0.82[CHB][hapmap];0.85[EUR][1000 genomes]
rs9886503	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817379	chr8:114338391-115011632	Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv831429	chr8:114438561-114595565	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:114509400-114511000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr8:114509600-114510800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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