Variant report

Variant	rs4763036
Chromosome Location	chr12:63224600-63224601
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11174687	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11174690	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11174693	0.87[EUR][1000 genomes]
rs12299234	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12303102	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12310765	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12314531	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12314598	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12314904	0.90[EUR][1000 genomes]
rs12314963	0.81[AFR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12317932	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12321622	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12811245	1.00[CHB][hapmap]
rs12818573	1.00[CHB][hapmap]
rs17098378	1.00[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34031846	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4762981	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4763029	1.00[CHB][hapmap]
rs4763031	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4763032	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4763033	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4763039	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58144383	0.90[EUR][1000 genomes]
rs58419885	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60201508	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61032877	0.90[EUR][1000 genomes]
rs61921197	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61921199	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61922299	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61922302	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61922305	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61922306	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7311022	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7311342	1.00[CEU][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7316591	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7397471	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7397483	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs74097105	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7955839	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7968796	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7977929	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3401870	chr12:63215053-63228223	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63195800-63228600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:63196000-63225800	Weak transcription	Gastric	stomach
3	chr12:63207200-63228600	Weak transcription	A549	lung
4	chr12:63207200-63231200	Weak transcription	Pancreas	Pancrea
5	chr12:63211800-63228000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr12:63211800-63228200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:63211800-63228200	Weak transcription	Aorta	Aorta
8	chr12:63212000-63225600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr12:63212000-63228200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr12:63212200-63227800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr12:63212400-63224600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr12:63212400-63228200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr12:63212400-63228200	Weak transcription	Brain Cingulate Gyrus	brain
14	chr12:63212400-63228400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr12:63212400-63228600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr12:63212400-63228800	Weak transcription	Brain Anterior Caudate	brain
17	chr12:63212400-63229000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr12:63212600-63227200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr12:63212600-63234600	Weak transcription	Primary hematopoietic stem cells	blood
20	chr12:63213800-63225200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr12:63214000-63228400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr12:63214800-63227800	Weak transcription	Brain Substantia Nigra	brain
23	chr12:63218400-63234800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr12:63219400-63225000	Weak transcription	Liver	Liver
25	chr12:63219400-63226200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr12:63221000-63226400	Strong transcription	HepG2	liver
27	chr12:63221200-63226000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:63221200-63228200	Weak transcription	Ovary	ovary
29	chr12:63221400-63228800	Weak transcription	Fetal Kidney	kidney
30	chr12:63221600-63225800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr12:63221600-63234200	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr12:63222200-63226000	Weak transcription	Duodenum Mucosa	Duodenum
33	chr12:63222200-63228200	Weak transcription	Left Ventricle	heart
34	chr12:63222200-63235200	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr12:63222800-63226000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:63223000-63226200	Strong transcription	HUES6 Cell Line	embryonic stem cell
37	chr12:63223200-63226000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr12:63223600-63227400	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr12:63223800-63229200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr12:63224400-63225200	Strong transcription	Fetal Intestine Large	intestine
41	chr12:63224400-63225800	Strong transcription	HUES64 Cell Line	embryonic stem cell
42	chr12:63224400-63225800	Strong transcription	Fetal Intestine Small	intestine
43	chr12:63224400-63226000	Strong transcription	Brain Angular Gyrus	brain
44	chr12:63224400-63228000	Weak transcription	Adipose Nuclei	Adipose
45	chr12:63224600-63226000	Strong transcription	Brain Inferior Temporal Lobe	brain

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