Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11992833	0.87[AMR][1000 genomes]
rs11993474	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11994410	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57416148	0.87[AMR][1000 genomes]
rs57759707	0.87[AMR][1000 genomes]
rs57871763	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58020170	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58156571	0.87[AMR][1000 genomes]
rs59812763	0.87[AMR][1000 genomes]
rs73242921	0.87[AMR][1000 genomes]
rs73242933	0.87[AMR][1000 genomes]
rs73242959	0.87[AMR][1000 genomes]
rs73242967	0.87[AMR][1000 genomes]
rs73242968	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73242971	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73242973	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73242975	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73242979	1.00[EUR][1000 genomes]
rs73242981	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73242982	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73242984	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73242992	1.00[EUR][1000 genomes]
rs73244804	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv1023239	chr8:66775321-66904124	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv3390496	chr8:66775633-66782628	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:66777000-66782400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:66780400-66782200	Weak transcription	Primary B cells from peripheral blood	blood
3	chr8:66781600-66783600	Enhancers	K562	blood
4	chr8:66781800-66782400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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