Variant report

Variant	rs11032776
Chromosome Location	chr11:34609480-34609481
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:34607496..34609587-chr11:34610286..34612192,2	K562	blood:
2	chr11:34590888..34592461-chr11:34607850..34609578,2	MCF-7	breast:
3	chr11:34608832..34611723-chr11:34620873..34624079,3	K562	blood:
4	chr11:34608087..34610149-chr11:34610286..34613011,2	K562	blood:

Variant related genes	Relation type
ENSG00000255427	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs34503767	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv897211	chr11:34514941-34609541	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv897212	chr11:34523173-34621004	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv832116	chr11:34539536-34673900	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34606200-34609600	Enhancers	Fetal Intestine Large	intestine
2	chr11:34606400-34610200	Enhancers	Fetal Intestine Small	intestine
3	chr11:34606800-34609800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr11:34607200-34610000	Enhancers	Hela-S3	cervix
5	chr11:34607400-34609600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr11:34607400-34609600	Enhancers	Fetal Heart	heart
7	chr11:34607400-34609600	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr11:34607400-34609800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:34607600-34609800	Enhancers	NHEK	skin
10	chr11:34608000-34609600	Enhancers	Pancreas	Pancrea
11	chr11:34608000-34610000	Enhancers	HepG2	liver
12	chr11:34608000-34610200	Enhancers	Placenta	Placenta
13	chr11:34608200-34609600	Enhancers	Esophagus	oesophagus
14	chr11:34608200-34609600	Enhancers	Placenta Amnion	Placenta Amnion
15	chr11:34608200-34610800	Enhancers	K562	blood
16	chr11:34608200-34611800	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr11:34608400-34609600	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr11:34608400-34610000	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr11:34608400-34610200	Enhancers	A549	lung
20	chr11:34608400-34611400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr11:34608400-34613800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr11:34608400-34618400	Weak transcription	Duodenum Mucosa	Duodenum
23	chr11:34608400-34643600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr11:34609000-34609600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr11:34609000-34609600	Enhancers	NHDF-Ad	bronchial
26	chr11:34609200-34614200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr11:34609400-34610000	Enhancers	Primary monocytes fromperipheralblood	blood

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