Variant report

Variant	rs13152312
Chromosome Location	chr4:7971312-7971313
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:7965044..7967214-chr4:7970387..7972613,2	MCF-7	breast:
2	chr4:7938506..7945813-chr4:7968503..7977501,21	MCF-7	breast:
3	chr4:7941236..7944392-chr4:7970174..7972613,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000196526	Chromatin interaction
ENSG00000228919	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491712	chr4:7582506-8155069	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	esv34140	chr4:7787936-8172491	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
3	esv2754386	chr4:7822449-7992909	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2756298	chr4:7822449-7992909	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv829851	chr4:7958698-8049060	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
6	nsv469779	chr4:7965253-8177646	Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
7	nsv482448	chr4:7965253-8177646	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
8	nsv878579	chr4:7969594-8011696	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	7 gene(s)	inside rSNPs	diseases
9	esv18370	chr4:7971253-7974932	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7959400-7971600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:7963000-7971600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:7963200-7971600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:7963200-7971800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:7963400-7975400	Weak transcription	Aorta	Aorta
6	chr4:7964400-7971600	Enhancers	Primary T cells fromperipheralblood	blood
7	chr4:7966000-7971600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr4:7967000-7987600	Weak transcription	Psoas Muscle	Psoas
9	chr4:7968200-7972000	Enhancers	Fetal Intestine Large	intestine
10	chr4:7968600-7972000	Enhancers	Spleen	Spleen
11	chr4:7969000-7971600	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr4:7969000-7972000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr4:7969000-7975600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
14	chr4:7969200-7971600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr4:7969200-7972000	Enhancers	Stomach Mucosa	stomach
16	chr4:7969200-7972400	Enhancers	Colon Smooth Muscle	Colon
17	chr4:7969200-7973400	Enhancers	Right Ventricle	heart
18	chr4:7969200-7974400	Enhancers	Fetal Muscle Leg	muscle
19	chr4:7969200-7975600	Enhancers	Fetal Thymus	thymus
20	chr4:7969200-7975800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr4:7969400-7971600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr4:7969400-7971600	Enhancers	Hela-S3	cervix
23	chr4:7969400-7971800	Enhancers	Rectal Smooth Muscle	rectum
24	chr4:7969400-7972000	Enhancers	Placenta	Placenta
25	chr4:7969400-7972000	Enhancers	Fetal Stomach	stomach
26	chr4:7969400-7972400	Enhancers	Fetal Muscle Trunk	muscle
27	chr4:7969400-7972400	Enhancers	NHDF-Ad	bronchial
28	chr4:7969400-7972600	Enhancers	Left Ventricle	heart
29	chr4:7969400-7972800	Enhancers	Right Atrium	heart
30	chr4:7969400-7973200	Enhancers	NHLF	lung
31	chr4:7969400-7974800	Enhancers	Lung	lung
32	chr4:7969400-7975800	Enhancers	Stomach Smooth Muscle	stomach
33	chr4:7969400-7976000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr4:7969600-7971400	Weak transcription	Pancreas	Pancrea
35	chr4:7969600-7971400	Enhancers	HepG2	liver
36	chr4:7969600-7971600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr4:7969600-7971600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr4:7969600-7971600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr4:7969600-7971800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr4:7969600-7972000	Enhancers	Duodenum Mucosa	Duodenum
41	chr4:7969600-7975800	Enhancers	Placenta Amnion	Placenta Amnion
42	chr4:7969800-7971400	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr4:7969800-7971600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr4:7969800-7971600	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr4:7969800-7972000	Enhancers	Fetal Intestine Small	intestine
46	chr4:7969800-7972400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr4:7969800-7973600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr4:7970000-7971600	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr4:7970000-7971600	Weak transcription	HSMMtube	muscle
50	chr4:7970000-7971800	Weak transcription	Esophagus	oesophagus

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