Variant report

Variant	rs72960637
Chromosome Location	chr3:119022539-119022540
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:119014873..119018472-chr3:119020624..119023457,3	MCF-7	breast:
2	chr3:119016211..119028042-chr3:119037960..119043695,12	MCF-7	breast:

Variant related genes	Relation type
ENSG00000241155	Chromatin interaction
ENSG00000242829	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs4687849	1.00[EUR][1000 genomes]
rs4687850	1.00[EUR][1000 genomes]
rs4687999	1.00[EUR][1000 genomes]
rs6803331	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72960640	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72960642	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73854487	1.00[EUR][1000 genomes]
rs73854488	1.00[EUR][1000 genomes]
rs7646935	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9830421	0.94[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	esv3487859	chr3:118570588-119419623	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv3487860	chr3:118570588-119419623	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv829694	chr3:119011488-119153579	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:119014200-119029800	Weak transcription	Gastric	stomach
2	chr3:119014200-119032800	Weak transcription	Pancreas	Pancrea
3	chr3:119015000-119028600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr3:119015000-119041200	Weak transcription	Aorta	Aorta
5	chr3:119015200-119041000	Weak transcription	Fetal Kidney	kidney
6	chr3:119015800-119024400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr3:119015800-119024400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr3:119016000-119035400	Weak transcription	Fetal Brain Male	brain
9	chr3:119016000-119041000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr3:119016400-119024000	Weak transcription	Small Intestine	intestine
11	chr3:119016400-119040800	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr3:119016400-119041000	Weak transcription	Fetal Intestine Small	intestine
13	chr3:119016600-119024400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:119016600-119025000	Genic enhancers	Cortex derived primary cultured neurospheres	brain
15	chr3:119016800-119024800	Enhancers	Fetal Heart	heart
16	chr3:119017200-119023000	Weak transcription	Colon Smooth Muscle	Colon
17	chr3:119017200-119025000	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr3:119017400-119029800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr3:119017400-119040600	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr3:119017600-119032400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr3:119018800-119022600	Genic enhancers	Left Ventricle	heart
22	chr3:119018800-119032800	Weak transcription	Thymus	Thymus
23	chr3:119019000-119022600	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr3:119019200-119024800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr3:119019200-119024800	Genic enhancers	Fetal Stomach	stomach
26	chr3:119019200-119026000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr3:119019200-119040800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr3:119019400-119024200	Enhancers	Placenta	Placenta
29	chr3:119019600-119022600	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr3:119019600-119023600	Enhancers	HMEC	breast
31	chr3:119019600-119024800	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr3:119019800-119022600	Enhancers	Primary B cells from peripheral blood	blood
33	chr3:119020000-119022600	Enhancers	Primary hematopoietic stem cells	blood
34	chr3:119020000-119022600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:119020200-119022600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr3:119020200-119024400	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr3:119020400-119029800	Weak transcription	Colonic Mucosa	Colon
38	chr3:119020400-119040600	Weak transcription	Esophagus	oesophagus
39	chr3:119020600-119023000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr3:119020800-119030400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr3:119020800-119032400	Weak transcription	Fetal Muscle Trunk	muscle
42	chr3:119021000-119022600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr3:119021000-119027200	Weak transcription	Brain Substantia Nigra	brain
44	chr3:119021000-119030400	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr3:119021000-119032400	Weak transcription	Primary T cells from cord blood	blood
46	chr3:119021200-119041000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr3:119021200-119041000	Weak transcription	Fetal Thymus	thymus
48	chr3:119021400-119024000	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr3:119021600-119022600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr3:119021600-119022600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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