Variant report

Variant	rs13107837
Chromosome Location	chr4:16036112-16036113
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:16033674..16036542-chr4:16143122..16145633,2	MCF-7	breast:
2	chr4:16035503..16038004-chr4:16044490..16046008,2	MCF-7	breast:
3	chr4:16026900..16029773-chr4:16034427..16036480,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs13117333	0.89[JPT][hapmap]
rs13128332	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13140264	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs1400770	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1400772	0.86[ASN][1000 genomes]
rs28711908	0.89[ASN][1000 genomes]
rs885289	0.84[CHB][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs950946	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012988	chr4:15597510-16091527	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv916742	chr4:15797994-16064232	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv998299	chr4:16031459-16226466	Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active 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 miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:16010800-16038600	Weak transcription	Placenta	Placenta
2	chr4:16025600-16045000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:16025600-16050600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr4:16025800-16057600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr4:16026400-16066600	Weak transcription	Colonic Mucosa	Colon
6	chr4:16026400-16066600	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr4:16027200-16039000	Weak transcription	Fetal Muscle Trunk	muscle
8	chr4:16030400-16039000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr4:16031200-16040000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr4:16032400-16036600	Enhancers	Fetal Brain Male	brain
11	chr4:16032800-16039800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr4:16033000-16037600	Enhancers	HepG2	liver
13	chr4:16033000-16039800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:16033200-16039200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:16033200-16039600	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr4:16033800-16036400	Enhancers	NH-A	brain
17	chr4:16033800-16038400	Weak transcription	Primary B cells from cord blood	blood
18	chr4:16034000-16036400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr4:16034000-16037000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr4:16034200-16036600	Enhancers	Fetal Heart	heart
21	chr4:16034400-16050400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:16034400-16072200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:16034600-16036200	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr4:16034600-16036200	Weak transcription	Brain Anterior Caudate	brain
25	chr4:16034800-16039000	Weak transcription	Fetal Muscle Leg	muscle
26	chr4:16034800-16039800	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr4:16035000-16036200	Weak transcription	Brain Germinal Matrix	brain
28	chr4:16035000-16039000	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr4:16035000-16042800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr4:16035000-16044800	Weak transcription	Fetal Brain Female	brain
31	chr4:16035200-16036400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:16035200-16036400	Enhancers	Liver	Liver
33	chr4:16035200-16036800	Enhancers	Stomach Mucosa	stomach
34	chr4:16035200-16037000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr4:16035200-16050800	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr4:16035200-16050800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr4:16035600-16036200	Enhancers	Muscle Satellite Cultured Cells	--
38	chr4:16035600-16036200	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr4:16035600-16036400	Active TSS	Aorta	Aorta
40	chr4:16035600-16036400	Enhancers	Fetal Stomach	stomach
41	chr4:16035600-16036400	Enhancers	NHEK	skin
42	chr4:16035600-16040000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:16035800-16036200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr4:16035800-16036200	Weak transcription	Fetal Intestine Small	intestine
45	chr4:16035800-16036200	Enhancers	HSMM	muscle
46	chr4:16035800-16036200	Flanking Active TSS	HSMMtube	muscle
47	chr4:16035800-16036200	Enhancers	NHDF-Ad	bronchial
48	chr4:16035800-16036200	Enhancers	Osteobl	bone
49	chr4:16035800-16036400	Genic enhancers	Primary hematopoietic stem cells	blood
50	chr4:16035800-16036600	Enhancers	Fetal Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links