Variant report

Variant	rs11224820
Chromosome Location	chr11:101402264-101402265
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11224823	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11224832	0.83[ASN][1000 genomes]
rs11224834	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs11224841	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs11224851	1.00[JPT][hapmap]
rs12361104	0.83[ASN][1000 genomes]
rs12785250	0.83[ASN][1000 genomes]
rs12791029	0.83[ASN][1000 genomes]
rs12792271	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs12793532	0.83[ASN][1000 genomes]
rs12798282	0.83[ASN][1000 genomes]
rs12800593	0.83[ASN][1000 genomes]
rs12800634	0.83[ASN][1000 genomes]
rs12801413	0.83[ASN][1000 genomes]
rs12802352	0.83[ASN][1000 genomes]
rs12803724	0.83[ASN][1000 genomes]
rs12806857	0.83[ASN][1000 genomes]
rs12807755	0.83[ASN][1000 genomes]
rs66638471	0.83[ASN][1000 genomes]
rs67343405	0.83[ASN][1000 genomes]
rs7119370	0.83[ASN][1000 genomes]
rs71462692	0.83[ASN][1000 genomes]
rs7926503	1.00[JPT][hapmap]

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	nsv556131	chr11:100985777-101480017	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv530644	chr11:101010088-101486038	Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv898330	chr11:101243644-101722031	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv556133	chr11:101398450-101433161	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv556134	chr11:101398450-101436689	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv556135	chr11:101399510-101436689	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101392400-101402600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr11:101401200-101425800	Weak transcription	Ovary	ovary

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