Variant report

Variant	rs3109781
Chromosome Location	chr8:85503236-85503237
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1252200	0.97[ASN][1000 genomes]
rs1252202	0.97[ASN][1000 genomes]
rs1252204	1.00[ASN][1000 genomes]
rs1252205	1.00[ASN][1000 genomes]
rs1252208	1.00[ASN][1000 genomes]
rs1252209	0.99[ASN][1000 genomes]
rs1252210	0.99[ASN][1000 genomes]
rs1252211	0.99[ASN][1000 genomes]
rs1252212	1.00[ASN][1000 genomes]
rs1252213	1.00[ASN][1000 genomes]
rs1252220	0.99[ASN][1000 genomes]
rs1252221	0.99[ASN][1000 genomes]
rs1252222	0.99[ASN][1000 genomes]
rs1252225	0.94[ASN][1000 genomes]
rs1268561	0.99[ASN][1000 genomes]
rs1268562	0.99[ASN][1000 genomes]
rs1351724	0.92[ASN][1000 genomes]
rs1466522	0.95[ASN][1000 genomes]
rs1483353	1.00[ASN][1000 genomes]
rs1483354	1.00[ASN][1000 genomes]
rs1626630	1.00[ASN][1000 genomes]
rs1681355	0.96[ASN][1000 genomes]
rs16913056	0.91[ASN][1000 genomes]
rs16913090	0.91[ASN][1000 genomes]
rs1730816	1.00[ASN][1000 genomes]
rs1730824	1.00[ASN][1000 genomes]
rs1730826	1.00[ASN][1000 genomes]
rs1730827	1.00[ASN][1000 genomes]
rs17794302	0.91[ASN][1000 genomes]
rs1842962	0.94[ASN][1000 genomes]
rs28405987	0.80[ASN][1000 genomes]
rs28446816	0.95[ASN][1000 genomes]
rs28676726	0.86[ASN][1000 genomes]
rs28695582	0.95[ASN][1000 genomes]
rs28760488	0.91[ASN][1000 genomes]
rs2930064	0.95[ASN][1000 genomes]
rs2957790	0.99[ASN][1000 genomes]
rs4302839	0.87[ASN][1000 genomes]
rs56165928	0.89[ASN][1000 genomes]
rs56335539	0.91[ASN][1000 genomes]
rs66683633	0.91[ASN][1000 genomes]
rs6997041	0.89[ASN][1000 genomes]
rs7014897	0.89[ASN][1000 genomes]
rs72681013	0.86[ASN][1000 genomes]
rs7819269	0.91[ASN][1000 genomes]
rs9886561	0.91[ASN][1000 genomes]
rs9987099	0.91[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	esv3481417	chr8:85279453-86145229	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	esv3481418	chr8:85279453-86145229	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 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	chr8:85498200-85516400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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