Variant report

Variant	rs12545796
Chromosome Location	chr8:131962578-131962579
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10090592	0.81[ASN][1000 genomes]
rs10090658	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10755934	0.81[ASN][1000 genomes]
rs10956563	0.84[ASN][1000 genomes]
rs10956565	0.81[ASN][1000 genomes]
rs10956566	0.81[ASN][1000 genomes]
rs10956567	0.81[ASN][1000 genomes]
rs11774077	1.00[JPT][hapmap]
rs11779492	1.00[JPT][hapmap]
rs11785068	1.00[JPT][hapmap]
rs11786442	1.00[JPT][hapmap]
rs11786761	0.81[ASN][1000 genomes]
rs12155837	0.81[ASN][1000 genomes]
rs12156272	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12335232	0.81[ASN][1000 genomes]
rs12550576	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12674666	0.81[ASN][1000 genomes]
rs28491358	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28576995	0.84[ASN][1000 genomes]
rs365538	1.00[JPT][hapmap]
rs4736462	0.94[ASN][1000 genomes]
rs4736463	0.81[ASN][1000 genomes]
rs4736726	0.81[ASN][1000 genomes]
rs4736727	0.81[ASN][1000 genomes]
rs4736728	0.81[ASN][1000 genomes]
rs4736729	0.81[ASN][1000 genomes]
rs4736730	0.81[ASN][1000 genomes]
rs59983985	0.81[ASN][1000 genomes]
rs6415525	0.81[ASN][1000 genomes]
rs6415526	0.81[ASN][1000 genomes]
rs6415527	0.81[ASN][1000 genomes]
rs6470870	0.81[ASN][1000 genomes]
rs6470871	0.81[ASN][1000 genomes]
rs6470872	0.81[ASN][1000 genomes]
rs6470873	0.81[ASN][1000 genomes]
rs6470874	0.84[ASN][1000 genomes]
rs6980986	0.81[ASN][1000 genomes]
rs6987081	0.81[ASN][1000 genomes]
rs6987663	0.81[ASN][1000 genomes]
rs6987807	0.81[ASN][1000 genomes]
rs6988340	0.81[ASN][1000 genomes]
rs6991107	0.81[ASN][1000 genomes]
rs6997190	0.81[ASN][1000 genomes]
rs6997744	0.81[ASN][1000 genomes]
rs6998224	0.81[ASN][1000 genomes]
rs7009300	0.81[ASN][1000 genomes]
rs7009319	0.81[ASN][1000 genomes]
rs7009351	0.81[ASN][1000 genomes]
rs7009501	0.81[ASN][1000 genomes]
rs7014446	0.81[ASN][1000 genomes]
rs7014917	0.81[ASN][1000 genomes]
rs7460718	0.81[ASN][1000 genomes]
rs7461026	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7828958	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891448	chr8:131668278-131968469	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	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
6	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
7	nsv972586	chr8:131956217-131962907	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:131961400-131968400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr8:131961600-131962600	Enhancers	Brain Germinal Matrix	brain
3	chr8:131961600-131962600	Weak transcription	Fetal Brain Male	brain
4	chr8:131962400-131962600	Bivalent Enhancer	Brain Hippocampus Middle	brain
5	chr8:131962400-131962800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr8:131962400-131963000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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