Variant report

Variant	rs11486184
Chromosome Location	chr1:153497906-153497907
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:153496118..153498124-chr1:153507716..153509971,2	K562	blood:
2	chr1:153483109..153485163-chr1:153497646..153499643,2	K562	blood:
3	chr1:153486911..153489748-chr1:153497891..153499485,2	MCF-7	breast:
4	chr1:153497091..153499956-chr1:153584552..153586138,2	MCF-7	breast:
5	chr1:153497834..153503028-chr1:153504169..153509062,7	MCF-7	breast:
6	chr1:153493940..153496088-chr1:153496990..153499406,2	K562	blood:

Variant related genes	Relation type
ENSG00000188643	Chromatin interaction
ENSG00000197956	Chromatin interaction
ENSG00000238279	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11486186	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010488	chr1:152901263-153670972	Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
2	nsv535171	chr1:152901263-153670972	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
3	nsv1002705	chr1:153307852-153525589	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
4	nsv831603	chr1:153405842-153576143	Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	148 gene(s)	inside rSNPs	diseases
5	nsv1007306	chr1:153413827-153541798	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153481200-153503600	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr1:153488600-153498200	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr1:153489000-153498000	Weak transcription	Esophagus	oesophagus
4	chr1:153489000-153498000	Weak transcription	Fetal Muscle Trunk	muscle
5	chr1:153489000-153506000	Weak transcription	Gastric	stomach
6	chr1:153489400-153498200	Weak transcription	Hela-S3	cervix
7	chr1:153491800-153498400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr1:153492000-153499200	Weak transcription	Fetal Thymus	thymus
9	chr1:153492400-153498400	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr1:153493000-153499400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr1:153493600-153498000	Weak transcription	Pancreas	Pancrea
12	chr1:153493600-153504000	Weak transcription	Colonic Mucosa	Colon
13	chr1:153493800-153498000	Weak transcription	Placenta	Placenta
14	chr1:153494000-153498200	Weak transcription	Duodenum Mucosa	Duodenum
15	chr1:153494200-153498000	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr1:153495400-153498000	Weak transcription	Fetal Intestine Small	intestine
17	chr1:153495600-153498000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr1:153495600-153498000	Weak transcription	Fetal Intestine Large	intestine
19	chr1:153495600-153498200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:153495600-153504800	Weak transcription	Spleen	Spleen
21	chr1:153495800-153498400	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr1:153496800-153500800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr1:153497200-153500400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:153497200-153500600	Enhancers	HMEC	breast
25	chr1:153497200-153504600	Weak transcription	Stomach Smooth Muscle	stomach
26	chr1:153497400-153498200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:153497400-153498200	Enhancers	NHEK	skin
28	chr1:153497400-153500800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:153497800-153498000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:153497800-153498000	Enhancers	Aorta	Aorta
31	chr1:153497800-153498200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr1:153497800-153498200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr1:153497800-153498200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr1:153497800-153498200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr1:153497800-153498200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr1:153497800-153498200	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr1:153497800-153498200	Enhancers	Osteobl	bone
38	chr1:153497800-153498400	Enhancers	Placenta Amnion	Placenta Amnion
39	chr1:153497800-153498400	Enhancers	K562	blood
40	chr1:153497800-153498600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr1:153497800-153498600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:153497800-153498800	Enhancers	H9 Cell Line	embryonic stem cell
43	chr1:153497800-153499000	Enhancers	HUVEC	blood vessel
44	chr1:153497800-153499600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:153497800-153499600	Enhancers	Fetal Muscle Leg	muscle
46	chr1:153497800-153499800	Enhancers	HepG2	liver
47	chr1:153497800-153500000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr1:153497800-153500000	Enhancers	NHLF	lung
49	chr1:153497800-153500400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr1:153497800-153500400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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