Variant report

Variant	rs711060
Chromosome Location	chr8:85457894-85457895
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs1021852	1.00[JPT][hapmap]
rs1021853	1.00[JPT][hapmap]
rs1039520	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10504803	0.95[CHD][hapmap];1.00[JPT][hapmap]
rs10504805	0.85[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs12114244	1.00[JPT][hapmap]
rs1319379	1.00[JPT][hapmap]
rs1320769	1.00[ASN][1000 genomes]
rs1320770	1.00[ASN][1000 genomes]
rs13248532	1.00[JPT][hapmap]
rs13250018	0.89[ASN][1000 genomes]
rs13252091	0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap]
rs13253537	1.00[JPT][hapmap]
rs13255463	1.00[JPT][hapmap]
rs13264793	0.98[ASN][1000 genomes]
rs1351223	0.86[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap]
rs1393990	1.00[ASW][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.96[YRI][hapmap]
rs1479092	1.00[JPT][hapmap]
rs1479093	1.00[JPT][hapmap]
rs1479094	0.95[JPT][hapmap]
rs1479096	0.95[JPT][hapmap]
rs1479098	1.00[JPT][hapmap]
rs1503600	1.00[ASN][1000 genomes]
rs1503601	0.99[ASN][1000 genomes]
rs1564314	0.95[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap]
rs1564315	1.00[JPT][hapmap]
rs1564316	1.00[JPT][hapmap]
rs1566791	0.95[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap]
rs1566792	1.00[JPT][hapmap]
rs1824887	1.00[JPT][hapmap]
rs1847344	1.00[CHB][hapmap];0.95[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1947960	1.00[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1994149	0.83[JPT][hapmap]
rs2046313	0.91[ASN][1000 genomes]
rs2127218	1.00[JPT][hapmap]
rs2169922	1.00[JPT][hapmap]
rs317947	0.92[CEU][hapmap];0.85[JPT][hapmap]
rs4739691	0.95[CHD][hapmap];1.00[JPT][hapmap]
rs4740015	1.00[JPT][hapmap]
rs4740016	1.00[JPT][hapmap]
rs4740018	0.80[CHB][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap]
rs4740019	1.00[JPT][hapmap]
rs4740023	0.95[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4740024	0.82[ASN][1000 genomes]
rs60533047	0.82[ASN][1000 genomes]
rs6473553	1.00[JPT][hapmap]
rs6473554	1.00[JPT][hapmap]
rs6473555	0.89[ASN][1000 genomes]
rs7011638	1.00[JPT][hapmap]
rs7013087	0.95[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap]
rs711002	0.81[CEU][hapmap];0.85[JPT][hapmap]
rs711006	0.84[CEU][hapmap];0.85[JPT][hapmap]
rs711007	0.83[ASW][hapmap];0.88[CEU][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.83[TSI][hapmap]
rs711009	0.84[CEU][hapmap]
rs711011	1.00[JPT][hapmap]
rs711012	0.84[CEU][hapmap];0.83[TSI][hapmap]
rs711014	0.84[CEU][hapmap];0.83[TSI][hapmap]
rs711017	0.84[CEU][hapmap]
rs711021	0.83[CEU][hapmap]
rs711025	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs711026	0.84[CEU][hapmap]
rs711027	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs711030	0.83[CEU][hapmap]
rs711032	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs711033	1.00[CEU][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap]
rs711041	1.00[CEU][hapmap];0.95[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap]
rs711048	1.00[CEU][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap]
rs711051	0.84[CEU][hapmap]
rs711052	1.00[CEU][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs711054	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs711059	1.00[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7820792	0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7822198	1.00[JPT][hapmap]
rs7822220	1.00[JPT][hapmap]
rs783507	0.92[CEU][hapmap];0.84[GIH][hapmap];0.85[JPT][hapmap];0.91[MEX][hapmap];0.84[TSI][hapmap]
rs783508	0.92[CEU][hapmap];0.85[JPT][hapmap]
rs783509	0.81[CEU][hapmap];0.81[GIH][hapmap];0.85[JPT][hapmap]
rs783787	0.84[CEU][hapmap]
rs783788	0.81[CEU][hapmap];0.85[JPT][hapmap]
rs783789	0.81[CEU][hapmap];0.85[JPT][hapmap]
rs783791	0.81[CEU][hapmap];0.85[JPT][hapmap]
rs7845599	1.00[JPT][hapmap]
rs9298424	0.83[ASW][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap]

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	nsv831375	chr8:85272352-85463621	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	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
3	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	chr8:85436200-85461200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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