Variant report

Variant	rs4763033
Chromosome Location	chr12:63223905-63223906
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	chr12:63222256..63224492-chr12:63227398..63230235,3	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs11174687	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11174690	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11174693	0.84[EUR][1000 genomes]
rs12299234	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12303102	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12310765	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12314531	0.81[ASN][1000 genomes]
rs12314598	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12314904	0.87[EUR][1000 genomes]
rs12314963	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12317932	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12321622	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17098378	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34031846	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4762981	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4763031	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4763032	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4763036	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4763039	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58144383	0.87[EUR][1000 genomes]
rs58419885	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60201508	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61032877	0.87[EUR][1000 genomes]
rs61921197	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61921199	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61922299	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61922302	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61922305	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61922306	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7311022	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7311342	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7316591	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7397471	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7397483	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74097105	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7955839	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7968796	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7977929	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[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:43 , 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	chr12:63212400-63224400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr12:63212400-63224600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr12:63212400-63228200	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr12:63212400-63228200	Weak transcription	Brain Cingulate Gyrus	brain
15	chr12:63212400-63228400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr12:63212400-63228600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr12:63212400-63228800	Weak transcription	Brain Anterior Caudate	brain
18	chr12:63212400-63229000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr12:63212600-63227200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr12:63212600-63234600	Weak transcription	Primary hematopoietic stem cells	blood
21	chr12:63213800-63225200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr12:63214000-63228400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr12:63214400-63224400	Weak transcription	Fetal Intestine Small	intestine
24	chr12:63214800-63227800	Weak transcription	Brain Substantia Nigra	brain
25	chr12:63218400-63234800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr12:63218800-63224400	Weak transcription	Fetal Intestine Large	intestine
27	chr12:63219400-63225000	Weak transcription	Liver	Liver
28	chr12:63219400-63226200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr12:63221000-63226400	Strong transcription	HepG2	liver
30	chr12:63221200-63226000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr12:63221200-63228200	Weak transcription	Ovary	ovary
32	chr12:63221400-63228800	Weak transcription	Fetal Kidney	kidney
33	chr12:63221600-63225800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr12:63221600-63234200	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr12:63222000-63224400	Weak transcription	Brain Angular Gyrus	brain
36	chr12:63222200-63226000	Weak transcription	Duodenum Mucosa	Duodenum
37	chr12:63222200-63228200	Weak transcription	Left Ventricle	heart
38	chr12:63222200-63235200	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr12:63222800-63226000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr12:63223000-63226200	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr12:63223200-63226000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr12:63223600-63227400	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr12:63223800-63229200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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