Variant report

Variant	rs7693116
Chromosome Location	chr4:76595774-76595775
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:76595601..76600505-chr4:76645864..76652704,29	K562	blood:
2	chr4:76593006..76595820-chr4:76737546..76740383,2	K562	blood:
3	chr4:76594895..76597627-chr4:76694798..76696348,2	K562	blood:
4	chr4:76595422..76600363-chr4:76647674..76651574,9	MCF-7	breast:
5	chr4:76594283..76597057-chr4:77067982..77070334,2	K562	blood:

Variant related genes	Relation type
ENSG00000138750	Chromatin interaction
ENSG00000138757	Chromatin interaction
ENSG00000138768	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10856862	1.00[EUR][1000 genomes]
rs13149236	1.00[EUR][1000 genomes]
rs1546567	1.00[EUR][1000 genomes]
rs1546568	1.00[EUR][1000 genomes]
rs17000609	1.00[EUR][1000 genomes]
rs17000707	1.00[EUR][1000 genomes]
rs17000735	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17000764	1.00[EUR][1000 genomes]
rs17000810	1.00[EUR][1000 genomes]
rs17000961	1.00[EUR][1000 genomes]
rs17000973	1.00[EUR][1000 genomes]
rs17001036	1.00[EUR][1000 genomes]
rs17001150	1.00[EUR][1000 genomes]
rs17001165	1.00[EUR][1000 genomes]
rs2174513	1.00[EUR][1000 genomes]
rs28406977	1.00[EUR][1000 genomes]
rs34155925	1.00[EUR][1000 genomes]
rs4324568	1.00[EUR][1000 genomes]
rs4859563	1.00[EUR][1000 genomes]
rs5028031	1.00[EUR][1000 genomes]
rs56024633	1.00[EUR][1000 genomes]
rs57659593	1.00[EUR][1000 genomes]
rs61288563	1.00[EUR][1000 genomes]
rs6531992	1.00[EUR][1000 genomes]
rs6811934	1.00[EUR][1000 genomes]
rs6816985	1.00[EUR][1000 genomes]
rs6824610	1.00[EUR][1000 genomes]
rs6825648	1.00[EUR][1000 genomes]
rs6826893	1.00[EUR][1000 genomes]
rs6838414	1.00[EUR][1000 genomes]
rs6844961	1.00[EUR][1000 genomes]
rs6856987	1.00[EUR][1000 genomes]
rs73825563	1.00[EUR][1000 genomes]
rs73825569	1.00[EUR][1000 genomes]
rs73825570	1.00[EUR][1000 genomes]
rs7654738	1.00[EUR][1000 genomes]
rs7685485	1.00[EUR][1000 genomes]
rs7685710	1.00[EUR][1000 genomes]
rs7694950	1.00[EUR][1000 genomes]
rs9998204	1.00[EUR][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	nsv879496	chr4:76493256-76620803	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv879497	chr4:76519096-76620803	Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	esv3353539	chr4:76530136-76993859	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76566200-76596600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:76567400-76596600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr4:76573800-76596200	Weak transcription	Colonic Mucosa	Colon
4	chr4:76574000-76596400	Weak transcription	Right Ventricle	heart
5	chr4:76578000-76596400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr4:76578000-76597000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:76578000-76597000	Weak transcription	Esophagus	oesophagus
8	chr4:76583400-76595800	Weak transcription	Brain Hippocampus Middle	brain
9	chr4:76583400-76595800	Weak transcription	Fetal Kidney	kidney
10	chr4:76583400-76596200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr4:76583400-76596200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr4:76583600-76596200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:76583800-76596200	Weak transcription	Brain Substantia Nigra	brain
14	chr4:76584400-76596000	Weak transcription	Stomach Smooth Muscle	stomach
15	chr4:76584400-76596200	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr4:76584400-76596600	Weak transcription	HSMMtube	muscle
17	chr4:76584600-76596400	Weak transcription	Brain Angular Gyrus	brain
18	chr4:76584600-76597200	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr4:76585200-76596000	Weak transcription	NHLF	lung
20	chr4:76586600-76597400	Weak transcription	Gastric	stomach
21	chr4:76586800-76596000	Weak transcription	Fetal Lung	lung
22	chr4:76586800-76596400	Weak transcription	HSMM	muscle
23	chr4:76586800-76597000	Weak transcription	Fetal Muscle Trunk	muscle
24	chr4:76586800-76597200	Weak transcription	Lung	lung
25	chr4:76587000-76597000	Weak transcription	Fetal Muscle Leg	muscle
26	chr4:76587200-76596000	Weak transcription	Fetal Stomach	stomach
27	chr4:76587200-76596400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:76587200-76596400	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr4:76587400-76597000	Weak transcription	Placenta	Placenta
30	chr4:76588000-76596200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr4:76588000-76596200	Weak transcription	HMEC	breast
32	chr4:76588000-76596400	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr4:76588200-76596000	Weak transcription	Osteobl	bone
34	chr4:76588200-76596200	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr4:76588600-76596000	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr4:76588800-76596000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:76589200-76596600	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr4:76589400-76596200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr4:76589800-76596000	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr4:76590400-76596000	Enhancers	HepG2	liver
41	chr4:76590800-76596000	Weak transcription	Right Atrium	heart
42	chr4:76590800-76596200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr4:76590800-76597600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr4:76591200-76596000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr4:76591400-76596200	Weak transcription	NHDF-Ad	bronchial
46	chr4:76591600-76595800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:76592000-76596600	Enhancers	Fetal Intestine Large	intestine
48	chr4:76592200-76595800	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr4:76592200-76595800	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr4:76592400-76596800	Enhancers	Fetal Heart	heart

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