Variant report

Variant	rs7295580
Chromosome Location	chr12:48492193-48492194
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	chr12:48490196..48492740-chr12:48498056..48500665,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000152556	Chromatin interaction
ENSG00000079387	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10161358	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10875743	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10875749	0.82[EUR][1000 genomes]
rs11168408	0.84[EUR][1000 genomes]
rs12228750	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1476607	0.82[EUR][1000 genomes]
rs2051851	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3997	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4760679	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7139330	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7301003	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8716	0.81[EUR][1000 genomes]
rs973398	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9971924	0.89[AMR][1000 genomes];0.90[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	esv2758307	chr12:48429702-48825499	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	esv2759898	chr12:48429702-48825499	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS 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 miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv508673	chr12:48489786-48567138	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7295580	RP1-228P16.1	cis	Artery Tibial	GTEx

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48432200-48498400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:48453000-48498200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr12:48454000-48494000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:48468600-48498400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:48468800-48498200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr12:48470200-48497600	Weak transcription	Fetal Heart	heart
7	chr12:48470800-48492800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:48472600-48493600	Strong transcription	Fetal Thymus	thymus
9	chr12:48472800-48493800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr12:48473000-48494800	Strong transcription	Primary T helper cells fromperipheralblood	blood
11	chr12:48473600-48495400	Strong transcription	Dnd41	blood
12	chr12:48473800-48492800	Strong transcription	Primary T helper cells PMA-I stimulated	--
13	chr12:48474000-48493000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr12:48474000-48494800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr12:48474600-48492200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr12:48475000-48498200	Weak transcription	Psoas Muscle	Psoas
17	chr12:48476800-48498400	Weak transcription	Fetal Brain Male	brain
18	chr12:48477200-48498200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr12:48477400-48498400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr12:48478600-48492200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr12:48478600-48493600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr12:48478800-48492200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr12:48479400-48498200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr12:48479400-48498200	Weak transcription	Brain Angular Gyrus	brain
25	chr12:48479400-48498400	Weak transcription	Aorta	Aorta
26	chr12:48479600-48498000	Weak transcription	NHEK	skin
27	chr12:48480000-48492800	Strong transcription	K562	blood
28	chr12:48480400-48498200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr12:48480800-48493600	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr12:48481200-48493800	Strong transcription	Stomach Smooth Muscle	stomach
31	chr12:48482800-48498200	Weak transcription	NHDF-Ad	bronchial
32	chr12:48483000-48498200	Weak transcription	NH-A	brain
33	chr12:48483000-48498400	Weak transcription	HSMMtube	muscle
34	chr12:48483200-48498200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr12:48483200-48498200	Weak transcription	HepG2	liver
36	chr12:48483200-48498400	Weak transcription	Brain Cingulate Gyrus	brain
37	chr12:48483200-48499200	Weak transcription	Small Intestine	intestine
38	chr12:48483400-48498200	Weak transcription	NHLF	lung
39	chr12:48484400-48492400	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr12:48484600-48492200	Strong transcription	Primary B cells from peripheral blood	blood
41	chr12:48484800-48498200	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr12:48485000-48498200	Weak transcription	Spleen	Spleen
43	chr12:48486200-48499000	Weak transcription	Gastric	stomach
44	chr12:48486400-48497800	Weak transcription	Primary hematopoietic stem cells	blood
45	chr12:48487200-48492400	Strong transcription	Fetal Muscle Trunk	muscle
46	chr12:48487200-48493600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr12:48487200-48494400	Strong transcription	Fetal Stomach	stomach
48	chr12:48488000-48496800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr12:48488000-48498200	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr12:48488200-48495400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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