Variant report

Variant	rs182869495
Chromosome Location	chr15:29983451-29983452
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:29983051..29984598-chr15:30024023..30026061,2	MCF-7	breast:
2	chr15:29978882..29981352-chr15:29982247..29985034,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000104067	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv456736	chr15:29327352-30208654	Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv568675	chr15:29327352-30208654	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv903747	chr15:29361126-30008977	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv995038	chr15:29744279-30366124	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv1038495	chr15:29825859-30351687	Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv542293	chr15:29825859-30351687	Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
7	nsv832944	chr15:29861062-30082057	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv832945	chr15:29932599-30123721	Genic enhancers Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
9	nsv974492	chr15:29981646-29991999	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	esv18527	chr15:29983142-29983647	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:29969200-29992000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr15:29972800-29989200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr15:29973600-29989600	Weak transcription	Fetal Muscle Leg	muscle
4	chr15:29977800-29996200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr15:29978400-29990400	Weak transcription	NHLF	lung
6	chr15:29978600-29984800	Weak transcription	NHDF-Ad	bronchial
7	chr15:29979200-29988400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr15:29979800-29993000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr15:29980800-29989800	Weak transcription	Brain Substantia Nigra	brain
10	chr15:29980800-29989800	Weak transcription	Fetal Kidney	kidney
11	chr15:29980800-29996400	Weak transcription	Colonic Mucosa	Colon
12	chr15:29981000-29990400	Weak transcription	Lung	lung
13	chr15:29981000-29990600	Weak transcription	Fetal Intestine Large	intestine
14	chr15:29981000-29994400	Weak transcription	Fetal Intestine Small	intestine
15	chr15:29981200-29989600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr15:29981200-29993000	Weak transcription	Duodenum Mucosa	Duodenum
17	chr15:29981400-29991800	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr15:29981400-29994800	Weak transcription	K562	blood
19	chr15:29981400-29996400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr15:29981600-29990400	Weak transcription	Esophagus	oesophagus
21	chr15:29981600-29990400	Weak transcription	Placenta	Placenta
22	chr15:29982000-29992000	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr15:29982800-29983600	Enhancers	Stomach Mucosa	stomach
24	chr15:29982800-29983600	Enhancers	NH-A	brain
25	chr15:29982800-29983800	Enhancers	Pancreas	Pancrea
26	chr15:29982800-29984000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr15:29982800-29984200	Enhancers	Liver	Liver
28	chr15:29983000-29983600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr15:29983000-29983800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr15:29983000-29983800	Strong transcription	Stomach Smooth Muscle	stomach
31	chr15:29983000-29984000	Enhancers	HepG2	liver
32	chr15:29983000-29989600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr15:29983200-29983600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr15:29983200-29983600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr15:29983200-29983600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr15:29983200-29983600	Enhancers	Osteobl	bone
37	chr15:29983200-29983800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr15:29983200-29983800	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr15:29983200-29983800	Enhancers	HMEC	breast
40	chr15:29983200-29983800	Enhancers	HSMM	muscle
41	chr15:29983200-29983800	Enhancers	HUVEC	blood vessel
42	chr15:29983200-29983800	Enhancers	NHEK	skin
43	chr15:29983200-29984000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr15:29983200-29984000	Enhancers	Gastric	stomach
45	chr15:29983400-29983600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr15:29983400-29983600	Flanking Active TSS	A549	lung
47	chr15:29983400-29983600	Genic enhancers	HSMMtube	muscle
48	chr15:29983400-29983800	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr15:29983400-29984200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr15:29983400-29984800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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