Variant report

Variant	rs11032682
Chromosome Location	chr11:34443753-34443754
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:34434860..34437756-chr11:34441290..34444180,2	K562	blood:
2	chr11:34436609..34439398-chr11:34442555..34445370,2	MCF-7	breast:
3	chr11:34443552..34446459-chr11:34446644..34449623,2	MCF-7	breast:
4	chr11:34438694..34440989-chr11:34441788..34444701,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1008491	0.96[ASN][1000 genomes]
rs10836223	0.86[ASN][1000 genomes]
rs10836229	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10836230	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10836234	0.96[ASN][1000 genomes]
rs11032661	0.92[ASN][1000 genomes]
rs11032667	0.92[ASN][1000 genomes]
rs11032669	0.92[ASN][1000 genomes]
rs11032670	0.92[ASN][1000 genomes]
rs11032671	0.92[ASN][1000 genomes]
rs11032695	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11032726	0.89[ASN][1000 genomes]
rs12361866	0.92[ASN][1000 genomes]
rs12790004	0.92[ASN][1000 genomes]
rs12790378	0.92[ASN][1000 genomes]
rs12793666	1.00[ASN][1000 genomes]
rs12804506	0.92[ASN][1000 genomes]
rs12804689	0.92[ASN][1000 genomes]
rs12806377	0.92[ASN][1000 genomes]
rs12807961	0.96[ASN][1000 genomes]
rs12808450	0.96[ASN][1000 genomes]
rs1408041	0.89[ASN][1000 genomes]
rs17269903	0.89[ASN][1000 genomes]
rs17352313	0.92[ASN][1000 genomes]
rs2146962	0.89[ASN][1000 genomes]
rs2420386	0.89[ASN][1000 genomes]
rs34329347	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34533645	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35725681	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59090359	0.92[ASN][1000 genomes]
rs66679411	1.00[ASN][1000 genomes]
rs7118388	0.88[CEU][hapmap]
rs737254	0.89[ASN][1000 genomes]
rs873466	0.92[ASN][1000 genomes]
rs910089	0.92[ASN][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	nsv897205	chr11:34248229-34507213	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv897207	chr11:34253683-34621004	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv897208	chr11:34257064-34562247	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv897209	chr11:34309519-34548906	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv983151	chr11:34401342-34444667	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv832114	chr11:34424428-34607851	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11032682	CAT	cis	Whole Blood	GTEx
rs11032682	CAT	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34437200-34446200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr11:34438200-34448600	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr11:34438600-34443800	Weak transcription	Primary B cells from cord blood	blood
4	chr11:34440000-34444800	Weak transcription	Lung	lung
5	chr11:34440200-34443800	Weak transcription	Liver	Liver
6	chr11:34440200-34447000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr11:34440200-34447400	Weak transcription	Hela-S3	cervix
8	chr11:34440400-34443800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr11:34443400-34450000	Enhancers	Primary hematopoietic stem cells	blood
10	chr11:34443600-34443800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr11:34443600-34443800	Enhancers	Esophagus	oesophagus
12	chr11:34443600-34443800	Enhancers	Left Ventricle	heart
13	chr11:34443600-34443800	Enhancers	Right Atrium	heart
14	chr11:34443600-34444000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr11:34443600-34444200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr11:34443600-34444200	Enhancers	Fetal Thymus	thymus
17	chr11:34443600-34444200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr11:34443600-34445200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr11:34443600-34445400	Enhancers	Fetal Lung	lung
20	chr11:34443600-34445800	Enhancers	Adipose Nuclei	Adipose

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