Variant report

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

rs_ID	r²[population]
rs11249961	0.99[ASN][1000 genomes]
rs11783922	0.86[ASN][1000 genomes]
rs12114434	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12114435	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12114909	0.81[AFR][1000 genomes]
rs12114977	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12540961	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12548657	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12550323	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13251619	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13260533	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17150534	0.85[ASN][1000 genomes]
rs17150543	0.86[ASN][1000 genomes]
rs2048653	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2048654	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2409618	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs4840447	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4840448	0.96[ASN][1000 genomes]
rs6601383	1.00[CEU][hapmap]
rs6980545	0.83[ASN][1000 genomes]
rs6984624	0.86[ASN][1000 genomes]
rs6984939	0.83[ASN][1000 genomes]
rs6988507	0.86[ASN][1000 genomes]
rs7002962	0.85[ASN][1000 genomes]
rs7005902	1.00[CEU][hapmap]
rs7018379	0.86[ASN][1000 genomes]
rs7814068	0.89[EUR][1000 genomes]
rs7823438	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9657510	0.80[EUR][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	nsv530864	chr8:9097498-9914548	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	esv16865	chr8:9642195-9712807	Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9684200-9689000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:9687600-9688200	Active TSS	Brain Inferior Temporal Lobe	brain
3	chr8:9688000-9688200	Active TSS	HepG2	liver

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