Variant report

Variant	rs11217636
Chromosome Location	chr11:119893164-119893165
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:119893105..119894802-chr11:119896511..119898254,2	K562	blood:
2	chr11:119886138..119888688-chr11:119891563..119894396,2	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10431043	0.89[ASN][1000 genomes]
rs10892514	1.00[ASN][1000 genomes]
rs10892519	0.93[ASN][1000 genomes]
rs10892521	0.92[ASN][1000 genomes]
rs11217630	0.95[ASN][1000 genomes]
rs11217633	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11217635	0.99[ASN][1000 genomes]
rs11217637	1.00[ASN][1000 genomes]
rs11217647	0.94[ASN][1000 genomes]
rs11217665	0.88[ASN][1000 genomes]
rs11217666	0.88[ASN][1000 genomes]
rs12223988	1.00[ASN][1000 genomes]
rs12225953	0.88[ASN][1000 genomes]
rs12573999	0.93[ASN][1000 genomes]
rs12574203	0.96[ASN][1000 genomes]
rs12575245	0.90[ASN][1000 genomes]
rs56745971	1.00[ASN][1000 genomes]
rs56778655	0.99[ASN][1000 genomes]
rs57510602	0.99[ASN][1000 genomes]
rs57589469	0.93[ASN][1000 genomes]
rs58844530	0.89[ASN][1000 genomes]
rs60270569	0.92[ASN][1000 genomes]
rs60914924	0.81[ASN][1000 genomes]
rs60967975	0.99[ASN][1000 genomes]
rs61602379	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054057	chr11:119781953-120519770	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541178	chr11:119781953-120519770	Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv832285	chr11:119789595-119957724	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1037777	chr11:119842515-119898368	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv541179	chr11:119842515-119898368	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv524406	chr11:119873404-119893179	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv2762948	chr11:119876596-119901422	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv508657	chr11:119891578-119971212	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119883200-119893400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:119884800-119893600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:119884800-119893800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:119888200-119893400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:119888400-119893600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr11:119888800-119893400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr11:119888800-119893600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr11:119889000-119893200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr11:119889000-119893400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr11:119889000-119893400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr11:119889000-119893600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr11:119889000-119893600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr11:119891600-119893400	Enhancers	Fetal Intestine Small	intestine
14	chr11:119891800-119893400	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr11:119891800-119897000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:119892000-119893200	Enhancers	Fetal Intestine Large	intestine
17	chr11:119892000-119893800	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr11:119892200-119895400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr11:119892400-119893400	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr11:119892800-119894000	Weak transcription	Liver	Liver
21	chr11:119893000-119896000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr11:119893000-119896600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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