Variant report

Variant	rs74088715
Chromosome Location	chr12:48361523-48361524
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:48360838..48363620-chr12:48364578..48367184,3	K562	blood:
2	chr12:48360987..48363483-chr12:48393695..48396604,4	MCF-7	breast:
3	chr12:48356037..48360072-chr12:48360475..48364952,9	K562	blood:

Variant related genes	Relation type
ENSG00000134291	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10467100	1.00[EUR][1000 genomes]
rs11168264	1.00[EUR][1000 genomes]
rs11168288	1.00[EUR][1000 genomes]
rs11168290	1.00[EUR][1000 genomes]
rs11168368	1.00[EUR][1000 genomes]
rs11574002	1.00[EUR][1000 genomes]
rs11574017	1.00[AMR][1000 genomes]
rs11574060	1.00[EUR][1000 genomes]
rs11830088	1.00[EUR][1000 genomes]
rs11833896	1.00[EUR][1000 genomes]
rs11835282	1.00[EUR][1000 genomes]
rs11835720	1.00[EUR][1000 genomes]
rs11836542	1.00[EUR][1000 genomes]
rs11838217	1.00[EUR][1000 genomes]
rs12297117	1.00[EUR][1000 genomes]
rs1793947	1.00[EUR][1000 genomes]
rs34116679	1.00[EUR][1000 genomes]
rs34120080	1.00[EUR][1000 genomes]
rs34698661	1.00[EUR][1000 genomes]
rs35445616	1.00[EUR][1000 genomes]
rs35902603	1.00[EUR][1000 genomes]
rs41272745	1.00[EUR][1000 genomes]
rs41272751	1.00[EUR][1000 genomes]
rs41272757	1.00[EUR][1000 genomes]
rs41272761	1.00[EUR][1000 genomes]
rs56265470	1.00[EUR][1000 genomes]
rs57550917	1.00[EUR][1000 genomes]
rs57783574	1.00[EUR][1000 genomes]
rs58279970	1.00[EUR][1000 genomes]
rs58573495	1.00[EUR][1000 genomes]
rs59339937	1.00[EUR][1000 genomes]
rs60556433	1.00[EUR][1000 genomes]
rs60894356	1.00[EUR][1000 genomes]
rs7316602	1.00[EUR][1000 genomes]
rs73297147	1.00[EUR][1000 genomes]
rs73297150	1.00[EUR][1000 genomes]
rs73297159	1.00[EUR][1000 genomes]
rs74085216	1.00[EUR][1000 genomes]
rs74085221	1.00[EUR][1000 genomes]
rs74086446	1.00[EUR][1000 genomes]
rs74088779	1.00[EUR][1000 genomes]
rs7954412	1.00[EUR][1000 genomes]
rs7967673	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	nsv832401	chr12:48347453-48477999	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv519174	chr12:48359984-48365265	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv899061	chr12:48360620-48389023	Bivalent Enhancer Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48358200-48363200	Weak transcription	Brain Substantia Nigra	brain
2	chr12:48358200-48364200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr12:48358200-48366200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:48358200-48366200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr12:48358400-48362000	Weak transcription	Esophagus	oesophagus
6	chr12:48358400-48362400	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr12:48358400-48362400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr12:48358400-48362400	Weak transcription	Psoas Muscle	Psoas
9	chr12:48358400-48362800	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr12:48358400-48362800	Weak transcription	NH-A	brain
11	chr12:48358400-48364600	Weak transcription	Ovary	ovary
12	chr12:48358400-48365000	Weak transcription	Osteobl	bone
13	chr12:48358400-48365200	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr12:48358400-48366400	Weak transcription	Fetal Brain Male	brain
15	chr12:48358400-48367800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr12:48358400-48367800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr12:48358400-48369800	Weak transcription	Brain Angular Gyrus	brain
18	chr12:48358400-48373000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:48358600-48363000	Strong transcription	A549	lung
20	chr12:48358600-48363200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr12:48358600-48363400	Strong transcription	Fetal Thymus	thymus
22	chr12:48358600-48363600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr12:48358600-48363800	Weak transcription	Brain Hippocampus Middle	brain
24	chr12:48358600-48365200	Weak transcription	HSMMtube	muscle
25	chr12:48358600-48366600	Weak transcription	Fetal Lung	lung
26	chr12:48358600-48369400	Weak transcription	Fetal Kidney	kidney
27	chr12:48358600-48381400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:48358800-48362000	Weak transcription	Small Intestine	intestine
29	chr12:48358800-48366000	Weak transcription	HepG2	liver
30	chr12:48358800-48366200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr12:48359000-48362400	Strong transcription	NHEK	skin
32	chr12:48359000-48364000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:48359200-48361800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr12:48359200-48362800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr12:48359200-48363000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr12:48359200-48363000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr12:48359200-48363200	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr12:48359200-48363400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
39	chr12:48359200-48364000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr12:48359200-48364400	Strong transcription	Stomach Smooth Muscle	stomach
41	chr12:48359200-48364600	Strong transcription	Placenta	Placenta
42	chr12:48359200-48364800	Strong transcription	Primary T cells from cord blood	blood
43	chr12:48359200-48384000	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr12:48359400-48361800	Strong transcription	K562	blood
45	chr12:48359400-48362200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr12:48359400-48363200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr12:48359400-48363400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr12:48359600-48362400	Strong transcription	HMEC	breast
49	chr12:48359600-48363000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr12:48359600-48363200	Strong transcription	Primary hematopoietic stem cells	blood

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