Variant report

Variant	rs10090658
Chromosome Location	chr8:131976120-131976121
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10090592	0.85[ASN][1000 genomes]
rs10755934	0.85[ASN][1000 genomes]
rs10956563	0.81[ASN][1000 genomes]
rs10956565	0.85[ASN][1000 genomes]
rs10956566	0.85[ASN][1000 genomes]
rs11774077	1.00[JPT][hapmap]
rs11779492	1.00[JPT][hapmap]
rs11785068	1.00[JPT][hapmap]
rs11786442	1.00[JPT][hapmap]
rs11786761	0.85[ASN][1000 genomes]
rs12155837	0.85[ASN][1000 genomes]
rs12156272	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12545796	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12550576	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12674666	0.85[ASN][1000 genomes]
rs28491358	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28576995	0.81[ASN][1000 genomes]
rs365538	1.00[JPT][hapmap]
rs4736462	0.91[ASN][1000 genomes]
rs4736463	0.85[ASN][1000 genomes]
rs4736727	0.85[ASN][1000 genomes]
rs4736728	0.85[ASN][1000 genomes]
rs4736729	0.85[ASN][1000 genomes]
rs4736730	0.85[ASN][1000 genomes]
rs59983985	0.85[ASN][1000 genomes]
rs6415525	0.85[ASN][1000 genomes]
rs6415526	0.85[ASN][1000 genomes]
rs6415527	0.85[ASN][1000 genomes]
rs6470870	0.85[ASN][1000 genomes]
rs6470871	0.85[ASN][1000 genomes]
rs6470872	0.85[ASN][1000 genomes]
rs6470873	0.85[ASN][1000 genomes]
rs6470874	0.81[ASN][1000 genomes]
rs6987081	0.85[ASN][1000 genomes]
rs6987663	0.85[ASN][1000 genomes]
rs6987807	0.85[ASN][1000 genomes]
rs6988340	0.85[ASN][1000 genomes]
rs6991107	0.85[ASN][1000 genomes]
rs6997190	0.85[ASN][1000 genomes]
rs7009300	0.85[ASN][1000 genomes]
rs7009319	0.85[ASN][1000 genomes]
rs7009351	0.85[ASN][1000 genomes]
rs7009501	0.85[ASN][1000 genomes]
rs7014446	0.85[ASN][1000 genomes]
rs7014917	0.85[ASN][1000 genomes]
rs7460718	0.85[ASN][1000 genomes]
rs7461026	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7828958	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034107	chr8:131740146-131985765	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv539747	chr8:131740146-131985765	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1030881	chr8:131801472-132654822	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1028579	chr8:131909872-132497149	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1026579	chr8:131922531-132695045	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	esv2761471	chr8:131963290-132281905	Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:131968800-131976200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:131972800-131990200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr8:131975000-131976400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr8:131975000-131978200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:131975400-131976400	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr8:131975600-131976200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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