Variant report

Variant	rs12580702
Chromosome Location	chr12:51331917-51331918
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:51325095..51327824-chr12:51330132..51332828,3	K562	blood:
2	chr12:51331181..51333310-chr12:51354155..51356249,2	MCF-7	breast:
3	chr12:51325095..51328187-chr12:51330132..51332748,3	K562	blood:

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11169626	0.84[AFR][1000 genomes]
rs12809226	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12823317	0.87[EUR][1000 genomes]
rs2359187	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3414501	chr12:51174503-51534707	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats 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	67 gene(s)	inside rSNPs	diseases
2	esv34039	chr12:51326702-51671911	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:51319400-51346200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:51322200-51332600	Weak transcription	Fetal Kidney	kidney
3	chr12:51323000-51377200	Weak transcription	Aorta	Aorta
4	chr12:51328400-51332600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr12:51328800-51378000	Weak transcription	Brain Substantia Nigra	brain
6	chr12:51329200-51336200	Weak transcription	Stomach Smooth Muscle	stomach
7	chr12:51329200-51341600	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr12:51329600-51333200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr12:51329600-51373600	Weak transcription	Left Ventricle	heart
10	chr12:51330400-51332600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
11	chr12:51330600-51332800	Weak transcription	Liver	Liver
12	chr12:51330800-51332000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
13	chr12:51330800-51332200	ZNF genes & repeats	Fetal Thymus	thymus
14	chr12:51330800-51332400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr12:51330800-51332400	ZNF genes & repeats	Brain Germinal Matrix	brain
16	chr12:51330800-51332400	ZNF genes & repeats	Fetal Intestine Small	intestine
17	chr12:51330800-51332400	ZNF genes & repeats	Fetal Muscle Leg	muscle
18	chr12:51330800-51332600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
19	chr12:51330800-51332600	ZNF genes & repeats	Fetal Brain Female	brain
20	chr12:51331000-51332000	ZNF genes & repeats	Gastric	stomach
21	chr12:51331000-51332400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr12:51331000-51332400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr12:51331000-51332400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:51331000-51332400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr12:51331000-51332400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr12:51331000-51332400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
27	chr12:51331000-51332400	ZNF genes & repeats	Fetal Stomach	stomach
28	chr12:51331000-51332400	ZNF genes & repeats	Lung	lung
29	chr12:51331000-51332600	ZNF genes & repeats	Thymus	Thymus
30	chr12:51331000-51332600	ZNF genes & repeats	Dnd41	blood
31	chr12:51331000-51332800	ZNF genes & repeats	Primary B cells from cord blood	blood
32	chr12:51331400-51332000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr12:51331400-51332200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
34	chr12:51331400-51332400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:51331400-51332600	Strong transcription	Brain Angular Gyrus	brain
36	chr12:51331400-51332600	Weak transcription	Colon Smooth Muscle	Colon
37	chr12:51331400-51378400	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr12:51331600-51332400	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr12:51331600-51338000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr12:51331600-51373800	Weak transcription	Pancreas	Pancrea
41	chr12:51331800-51332400	Weak transcription	Fetal Muscle Trunk	muscle
42	chr12:51331800-51332600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr12:51331800-51333000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr12:51331800-51334400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr12:51331800-51342800	Weak transcription	Brain Hippocampus Middle	brain
46	chr12:51331800-51343000	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr12:51331800-51353800	Weak transcription	Primary T cells from cord blood	blood
48	chr12:51331800-51382000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr12:51331800-51382000	Weak transcription	Ovary	ovary

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