Variant report

Variant	rs7935453
Chromosome Location	chr11:8646763-8646764
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:8644589..8647498-chr11:8659025..8660844,2	MCF-7	breast:
2	chr11:8644859..8647194-chr11:8648029..8650090,2	K562	blood:
3	chr11:8641168..8642878-chr11:8644731..8647505,2	K562	blood:
4	chr11:8645853..8647429-chr11:8659220..8661284,2	K562	blood:
5	chr11:8645312..8647194-chr11:8647433..8649529,2	K562	blood:
6	chr11:8645853..8648717-chr11:8659784..8661524,2	K562	blood:
7	chr11:8524893..8527404-chr11:8645934..8647701,2	K562	blood:

Variant related genes	Relation type
ENSG00000166436	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10160373	0.95[ASN][1000 genomes]
rs10743084	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10769938	0.91[YRI][hapmap];0.82[AFR][1000 genomes]
rs11042019	0.94[ASN][1000 genomes]
rs11042033	0.91[ASN][1000 genomes]
rs12286011	0.89[ASN][1000 genomes]
rs12295729	0.99[ASN][1000 genomes]
rs12787554	0.95[CHB][hapmap];0.85[JPT][hapmap];0.92[ASN][1000 genomes]
rs13328833	0.95[ASN][1000 genomes]
rs3942866	0.90[JPT][hapmap]
rs57012665	0.88[ASN][1000 genomes]
rs7947230	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7950528	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751035	chr11:8431654-8685451	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv896983	chr11:8526643-8682465	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8626000-8661600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:8626000-8661800	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr11:8626200-8653000	Weak transcription	Rectal Smooth Muscle	rectum
4	chr11:8626600-8648800	Weak transcription	Stomach Mucosa	stomach
5	chr11:8626800-8659600	Weak transcription	Hela-S3	cervix
6	chr11:8630600-8653000	Weak transcription	Osteobl	bone
7	chr11:8632800-8659000	Weak transcription	Colon Smooth Muscle	Colon
8	chr11:8632800-8663800	Weak transcription	Fetal Kidney	kidney
9	chr11:8634000-8646800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:8634200-8647200	Strong transcription	Liver	Liver
11	chr11:8634600-8661600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr11:8634600-8661800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr11:8634800-8657600	Weak transcription	Psoas Muscle	Psoas
14	chr11:8635400-8646800	Weak transcription	Fetal Brain Male	brain
15	chr11:8635400-8647000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:8635400-8661400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr11:8635600-8647000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr11:8636200-8661400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr11:8636600-8657000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr11:8636800-8647000	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr11:8636800-8647200	Strong transcription	Stomach Smooth Muscle	stomach
22	chr11:8636800-8647400	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr11:8637000-8647200	Strong transcription	Fetal Intestine Small	intestine
24	chr11:8637000-8661600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr11:8637000-8703200	Weak transcription	Small Intestine	intestine
26	chr11:8637200-8646800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr11:8637200-8646800	Strong transcription	Placenta	Placenta
28	chr11:8637200-8646800	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr11:8637200-8647000	Strong transcription	Brain Inferior Temporal Lobe	brain
30	chr11:8637200-8647000	Strong transcription	Lung	lung
31	chr11:8637200-8647200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr11:8637200-8647200	Strong transcription	Aorta	Aorta
33	chr11:8637200-8647200	Strong transcription	Pancreas	Pancrea
34	chr11:8637200-8647200	Strong transcription	Skeletal Muscle Male	skeletal muscle
35	chr11:8637200-8647200	Strong transcription	Skeletal Muscle Female	skeletal muscle
36	chr11:8637200-8647400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr11:8637200-8647600	Strong transcription	Primary T cells from cord blood	blood
38	chr11:8637200-8647600	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr11:8637200-8648200	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr11:8637200-8648800	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr11:8637400-8646800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr11:8637400-8646800	Strong transcription	Rectal Mucosa Donor 31	rectum
43	chr11:8637400-8647000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr11:8637400-8647000	Strong transcription	Spleen	Spleen
45	chr11:8637400-8647600	Strong transcription	Adipose Nuclei	Adipose
46	chr11:8637400-8659200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:8637600-8646800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr11:8637600-8647000	Strong transcription	Dnd41	blood
49	chr11:8637600-8647400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr11:8637600-8647400	Strong transcription	Fetal Stomach	stomach

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