Variant report

Variant	rs12674666
Chromosome Location	chr8:131975445-131975446
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10090592	1.00[ASN][1000 genomes]
rs10090658	0.85[ASN][1000 genomes]
rs10755934	1.00[ASN][1000 genomes]
rs10956563	0.96[ASN][1000 genomes]
rs10956565	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10956566	1.00[ASN][1000 genomes]
rs10956567	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11774077	1.00[JPT][hapmap]
rs11775729	0.89[AFR][1000 genomes]
rs11779492	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs11785068	1.00[JPT][hapmap]
rs11786442	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs11786761	1.00[ASN][1000 genomes]
rs11995439	0.85[AFR][1000 genomes]
rs12155837	1.00[ASN][1000 genomes]
rs12156272	0.85[ASN][1000 genomes]
rs12335232	0.93[ASN][1000 genomes]
rs12545796	0.81[ASN][1000 genomes]
rs12550576	0.81[ASN][1000 genomes]
rs28491358	0.81[ASN][1000 genomes]
rs28576995	0.96[ASN][1000 genomes]
rs365538	1.00[JPT][hapmap]
rs4736463	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4736725	0.94[EUR][1000 genomes]
rs4736727	1.00[ASN][1000 genomes]
rs4736728	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4736729	1.00[ASN][1000 genomes]
rs4736730	1.00[ASN][1000 genomes]
rs59983985	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6415525	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6415526	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6415527	1.00[ASN][1000 genomes]
rs6470870	0.93[ASN][1000 genomes]
rs6470871	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6470872	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6470873	1.00[ASN][1000 genomes]
rs6470874	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6470875	0.89[ASN][1000 genomes]
rs6980986	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6986777	0.90[ASN][1000 genomes]
rs6987081	1.00[ASN][1000 genomes]
rs6987249	0.93[ASN][1000 genomes]
rs6987663	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6987807	1.00[ASN][1000 genomes]
rs6988340	1.00[ASN][1000 genomes]
rs6991107	1.00[ASN][1000 genomes]
rs6997190	1.00[ASN][1000 genomes]
rs6997744	0.93[ASN][1000 genomes]
rs6998224	0.93[ASN][1000 genomes]
rs7009300	1.00[ASN][1000 genomes]
rs7009319	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7009351	1.00[ASN][1000 genomes]
rs7009501	1.00[ASN][1000 genomes]
rs7014446	1.00[ASN][1000 genomes]
rs7014917	1.00[ASN][1000 genomes]
rs73718855	0.82[AFR][1000 genomes]
rs7460718	1.00[ASN][1000 genomes]
rs7461026	0.81[ASN][1000 genomes]
rs7828958	0.96[ASN][1000 genomes]
rs7830999	0.81[AFR][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:8 , 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	chr8:131973800-131975600	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr8:131974200-131975600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:131975000-131976400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr8:131975000-131978200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr8:131975200-131975600	Weak transcription	Brain Hippocampus Middle	brain
8	chr8:131975400-131976400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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