Variant report

Variant	rs11986452
Chromosome Location	chr8:20289797-20289798
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10111066	0.85[ASN][1000 genomes]
rs11204113	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11204115	0.84[ASN][1000 genomes]
rs11987582	0.83[ASN][1000 genomes]
rs12543148	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12543189	0.83[ASN][1000 genomes]
rs12550719	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12681299	0.84[ASN][1000 genomes]
rs13254166	0.83[ASN][1000 genomes]
rs13266470	0.83[ASN][1000 genomes]
rs13282008	0.84[ASN][1000 genomes]
rs17092415	0.86[ASN][1000 genomes]
rs17092418	0.86[ASN][1000 genomes]
rs17092433	0.84[ASN][1000 genomes]
rs1967996	0.85[ASN][1000 genomes]
rs2170176	0.83[ASN][1000 genomes]
rs2410646	0.85[ASN][1000 genomes]
rs2410647	0.85[ASN][1000 genomes]
rs2898502	0.83[ASN][1000 genomes]
rs35994919	0.86[ASN][1000 genomes]
rs4372014	0.83[ASN][1000 genomes]
rs4922192	0.81[EUR][1000 genomes]
rs4922198	0.86[ASN][1000 genomes]
rs4922199	0.84[ASN][1000 genomes]
rs57007589	0.86[ASN][1000 genomes]
rs62500019	0.85[ASN][1000 genomes]
rs6982875	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7387821	0.84[ASN][1000 genomes]
rs7814633	0.89[ASN][1000 genomes]
rs7817914	0.83[AFR][1000 genomes]
rs7829640	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7845281	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs900953	0.82[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	nsv1033511	chr8:19751299-20625091	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv530877	chr8:19873053-20593254	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv831256	chr8:20162233-20300224	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv2758152	chr8:20228949-20514807	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv2759603	chr8:20228949-20514807	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv469890	chr8:20239114-20445136	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv482881	chr8:20239114-20445136	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20280000-20291800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:20283200-20293000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr8:20287200-20292000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr8:20289600-20292600	Weak transcription	Stomach Mucosa	stomach

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