Variant report

Variant	rs9358049
Chromosome Location	chr6:15067276-15067277
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:15064020..15068777-chr6:15085229..15093631,19	MCF-7	breast:
2	chr6:15063509..15068597-chr6:15242568..15250230,12	MCF-7	breast:
3	chr6:15065231..15078374-chr6:15243362..15252213,26	MCF-7	breast:
4	chr6:14730821..14734594-chr6:15065015..15067705,5	MCF-7	breast:
5	chr6:15066128..15068160-chr6:15211246..15212780,2	K562	blood:
6	chr6:14741983..14744344-chr6:15066073..15067702,2	MCF-7	breast:
7	chr6:14737129..14739512-chr6:15065575..15068395,2	MCF-7	breast:
8	chr6:15063403..15067702-chr6:15220647..15223786,6	MCF-7	breast:
9	chr6:15065449..15068780-chr6:15072645..15074662,4	K562	blood:
10	chr6:15062744..15064596-chr6:15064785..15067869,4	K562	blood:
11	chr6:14887758..14891402-chr6:15064654..15067912,3	MCF-7	breast:
12	chr6:15065304..15068160-chr6:15210203..15212780,2	K562	blood:
13	chr6:15034583..15040875-chr6:15061503..15068528,12	MCF-7	breast:
14	chr6:15066460..15068940-chr6:15259945..15262215,2	MCF-7	breast:
15	chr6:15016924..15018771-chr6:15065604..15067583,2	K562	blood:
16	chr6:15065797..15068754-chr6:15078887..15080835,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000235488	Chromatin interaction
ENSG00000234261	Chromatin interaction
ENSG00000271888	Chromatin interaction
ENSG00000008083	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13190696	1.00[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	nsv883454	chr6:15009137-15081252	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv830593	chr6:15049636-15244190	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15043800-15077400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:15058200-15074400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:15061200-15069800	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr6:15065200-15067800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr6:15065200-15068600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr6:15065400-15067400	Enhancers	Fetal Lung	lung
7	chr6:15065400-15067600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:15065400-15067600	Enhancers	Fetal Stomach	stomach
9	chr6:15065400-15067600	Enhancers	Osteobl	bone
10	chr6:15065400-15067800	Enhancers	Muscle Satellite Cultured Cells	--
11	chr6:15065600-15067400	Enhancers	H9 Cell Line	embryonic stem cell
12	chr6:15065600-15067600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:15065600-15067600	Enhancers	HSMM	muscle
14	chr6:15065600-15067600	Enhancers	NH-A	brain
15	chr6:15065600-15067800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:15065600-15067800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr6:15065600-15067800	Enhancers	HMEC	breast
18	chr6:15065800-15067600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr6:15066000-15067600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr6:15066000-15067600	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr6:15066000-15067600	Enhancers	HSMMtube	muscle
22	chr6:15066000-15067800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr6:15066200-15067400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr6:15066600-15067600	Enhancers	HUVEC	blood vessel
25	chr6:15066800-15067400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr6:15066800-15067400	Enhancers	Primary hematopoietic stem cells	blood
27	chr6:15066800-15067400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr6:15066800-15067400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:15066800-15067400	Enhancers	Adipose Nuclei	Adipose
30	chr6:15066800-15067600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr6:15066800-15067600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
32	chr6:15066800-15067600	Enhancers	Esophagus	oesophagus
33	chr6:15066800-15067600	Flanking Active TSS	K562	blood
34	chr6:15066800-15067600	Enhancers	NHDF-Ad	bronchial
35	chr6:15066800-15067800	Enhancers	Placenta	Placenta
36	chr6:15067000-15067400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr6:15067000-15067400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr6:15067000-15067400	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr6:15067000-15067800	Enhancers	Spleen	Spleen
40	chr6:15067200-15067400	Flanking Active TSS	NHEK	skin
41	chr6:15067200-15067600	Enhancers	Stomach Mucosa	stomach
42	chr6:15067200-15076600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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