Variant report

Variant	rs896788
Chromosome Location	chr2:7149155-7149156
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:7147550..7151799-chr2:7153014..7155237,5	MCF-7	breast:
2	chr2:7055991..7058929-chr2:7148686..7150266,2	K562	blood:
3	chr2:7148867..7150372-chr2:7158852..7161810,2	MCF-7	breast:
4	chr2:7142289..7144797-chr2:7147566..7149207,2	K562	blood:
5	chr2:7142289..7146091-chr2:7146579..7150616,5	K562	blood:
6	chr2:7006003..7009208-chr2:7148136..7150396,3	MCF-7	breast:
7	chr2:7055201..7058278-chr2:7146257..7149807,3	MCF-7	breast:
8	chr2:7143200..7144893-chr2:7148159..7150235,2	MCF-7	breast:
9	chr2:7145702..7149842-chr2:7151104..7154625,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000151692	Chromatin interaction
ENSG00000134326	Chromatin interaction
ENSG00000228203	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12468736	0.84[EUR][1000 genomes]
rs12476611	0.84[EUR][1000 genomes]
rs13399156	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs13414682	0.90[ASN][1000 genomes]
rs35431985	0.84[EUR][1000 genomes]
rs3755507	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3771970	0.83[EUR][1000 genomes]
rs3771985	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3771990	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6720046	0.84[EUR][1000 genomes]
rs771260	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs771261	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs771270	0.83[ASN][1000 genomes]

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:7101200-7154000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr2:7124000-7157600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr2:7127200-7154000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr2:7131000-7167600	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr2:7131400-7150200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr2:7131400-7162400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr2:7131600-7154200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr2:7131600-7154200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr2:7133800-7150800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr2:7137200-7149800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr2:7137400-7160200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr2:7139600-7149800	Weak transcription	Ovary	ovary
13	chr2:7141800-7151200	Strong transcription	Primary T cells from cord blood	blood
14	chr2:7142600-7163000	Weak transcription	Small Intestine	intestine
15	chr2:7143600-7149200	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr2:7143800-7149200	Enhancers	Primary hematopoietic stem cells	blood
17	chr2:7143800-7150400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr2:7144200-7154600	Weak transcription	HepG2	liver
19	chr2:7144400-7150400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr2:7145000-7150600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr2:7145200-7156200	Enhancers	Brain Angular Gyrus	brain
22	chr2:7146400-7151200	Enhancers	Left Ventricle	heart
23	chr2:7146400-7153000	Enhancers	Right Ventricle	heart
24	chr2:7146600-7152800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr2:7146800-7149200	Enhancers	Lung	lung
26	chr2:7146800-7149400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr2:7146800-7150600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr2:7146800-7151200	Enhancers	Pancreas	Pancrea
29	chr2:7146800-7151200	Enhancers	Psoas Muscle	Psoas
30	chr2:7146800-7156000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr2:7147000-7154800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr2:7147200-7158600	Enhancers	Colon Smooth Muscle	Colon
33	chr2:7147400-7150800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:7147400-7151000	Enhancers	Fetal Thymus	thymus
35	chr2:7147400-7151200	Enhancers	Fetal Muscle Trunk	muscle
36	chr2:7147400-7151800	Enhancers	Rectal Smooth Muscle	rectum
37	chr2:7147400-7152200	Enhancers	NH-A	brain
38	chr2:7147400-7154000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr2:7147400-7156000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr2:7147400-7157000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr2:7147400-7159200	Weak transcription	Thymus	Thymus
42	chr2:7147600-7149200	Enhancers	Liver	Liver
43	chr2:7147600-7149200	Enhancers	Gastric	stomach
44	chr2:7147600-7149200	Flanking Active TSS	Stomach Smooth Muscle	stomach
45	chr2:7147600-7149400	Enhancers	Colonic Mucosa	Colon
46	chr2:7147600-7150600	Enhancers	Duodenum Mucosa	Duodenum
47	chr2:7147600-7155600	Enhancers	NHDF-Ad	bronchial
48	chr2:7147800-7149200	Enhancers	Placenta	Placenta
49	chr2:7147800-7149400	Enhancers	Stomach Mucosa	stomach
50	chr2:7148000-7150800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood

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