Variant report

Variant	rs11072264
Chromosome Location	chr15:33442996-33442997
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs1399079	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17816976	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4332721	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71462850	0.96[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv903979	chr15:33144202-33550256	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1052966	chr15:33149753-33541951	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv542340	chr15:33149753-33541951	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv903981	chr15:33207082-33550256	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv568918	chr15:33244672-33446971	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv903982	chr15:33282844-33616150	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv903983	chr15:33388030-33550256	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33427800-33445400	Weak transcription	Right Atrium	heart
2	chr15:33438400-33444800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr15:33438600-33449800	Weak transcription	NHEK	skin
4	chr15:33438800-33444600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr15:33439000-33445200	Weak transcription	Placenta	Placenta
6	chr15:33439000-33445200	Weak transcription	Lung	lung
7	chr15:33439000-33447200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr15:33441000-33443400	Weak transcription	Primary B cells from peripheral blood	blood
9	chr15:33441000-33444400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr15:33441000-33445200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr15:33441000-33445200	Weak transcription	Brain Angular Gyrus	brain
12	chr15:33441000-33447000	Weak transcription	Fetal Thymus	thymus
13	chr15:33441200-33444400	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr15:33441200-33444800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr15:33441200-33451800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr15:33441400-33443000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr15:33441600-33443400	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr15:33441600-33444000	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr15:33441800-33443800	Enhancers	Fetal Intestine Large	intestine
20	chr15:33442000-33443200	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr15:33442200-33444000	Enhancers	Fetal Intestine Small	intestine
22	chr15:33442200-33444200	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr15:33442200-33447600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr15:33442200-33447600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr15:33442600-33443000	Flanking Active TSS	Fetal Kidney	kidney
26	chr15:33442600-33443600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr15:33442600-33444400	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr15:33442600-33444600	Weak transcription	HMEC	breast
29	chr15:33442600-33448000	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr15:33442800-33443000	Enhancers	Duodenum Mucosa	Duodenum
31	chr15:33442800-33443200	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr15:33442800-33443200	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr15:33442800-33443400	Enhancers	Primary hematopoietic stem cells	blood
34	chr15:33442800-33444800	Weak transcription	Osteobl	bone
35	chr15:33442800-33445200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr15:33442800-33445400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr15:33442800-33447400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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