Variant report

Variant	rs60632886
Chromosome Location	chr5:94871175-94871176
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	chr5:94863895..94866493-chr5:94869547..94872168,2	K562	blood:
2	chr5:94869385..94872836-chr5:94884055..94887302,3	K562	blood:

Variant related genes	Relation type
ENSG00000198677	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11949777	0.89[AFR][1000 genomes]
rs11951853	0.83[AFR][1000 genomes]
rs17084844	0.89[AFR][1000 genomes]
rs17084856	0.84[AFR][1000 genomes]
rs17084871	0.84[AFR][1000 genomes]
rs17084888	0.83[AFR][1000 genomes]
rs17084908	0.89[AFR][1000 genomes]
rs17084925	0.83[AFR][1000 genomes]
rs2881774	0.89[AFR][1000 genomes]
rs56742088	0.83[AFR][1000 genomes]
rs57414975	0.89[AFR][1000 genomes]
rs57520226	0.83[AFR][1000 genomes]
rs58364348	0.83[AFR][1000 genomes]
rs59601824	0.83[AFR][1000 genomes]
rs73147905	0.94[AFR][1000 genomes]
rs73147915	0.94[AFR][1000 genomes]
rs73147917	0.94[AFR][1000 genomes]
rs73147919	0.94[AFR][1000 genomes]
rs73147928	0.84[AFR][1000 genomes]
rs73147929	0.94[AFR][1000 genomes]
rs73147938	0.89[AFR][1000 genomes]
rs73147967	0.83[AFR][1000 genomes]
rs73147968	0.89[AFR][1000 genomes]
rs73147970	0.83[AFR][1000 genomes]
rs7708692	0.94[AFR][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	nsv882388	chr5:94764006-94925849	Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94811000-94889400	Weak transcription	Stomach Mucosa	stomach
2	chr5:94818000-94882400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr5:94825000-94886200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr5:94825400-94886400	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr5:94826000-94886400	Strong transcription	Primary T helper cells fromperipheralblood	blood
6	chr5:94826800-94886400	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr5:94827200-94889600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr5:94828600-94873600	Strong transcription	Primary T helper cells PMA-I stimulated	--
9	chr5:94828800-94885800	Strong transcription	Fetal Thymus	thymus
10	chr5:94835200-94881000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr5:94841400-94883400	Strong transcription	Primary B cells from cord blood	blood
12	chr5:94841800-94886000	Strong transcription	Primary T cells fromperipheralblood	blood
13	chr5:94842000-94873600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr5:94842000-94884800	Strong transcription	Dnd41	blood
15	chr5:94842200-94882000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:94842200-94886000	Strong transcription	Primary B cells from peripheral blood	blood
17	chr5:94845600-94879800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr5:94846600-94881000	Weak transcription	Gastric	stomach
19	chr5:94847400-94890000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr5:94849200-94890000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr5:94849400-94871400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr5:94849800-94872000	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr5:94849800-94878200	Weak transcription	Fetal Intestine Small	intestine
24	chr5:94849800-94879800	Weak transcription	Fetal Stomach	stomach
25	chr5:94849800-94881400	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr5:94850600-94879200	Weak transcription	Small Intestine	intestine
27	chr5:94851800-94881200	Weak transcription	Right Ventricle	heart
28	chr5:94853800-94879800	Weak transcription	Lung	lung
29	chr5:94853800-94880400	Weak transcription	Pancreas	Pancrea
30	chr5:94853800-94890000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr5:94855800-94878400	Strong transcription	Liver	Liver
32	chr5:94857600-94884800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr5:94860600-94875800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr5:94863000-94872800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr5:94863000-94874600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr5:94864400-94889400	Weak transcription	Rectal Smooth Muscle	rectum
37	chr5:94865000-94872400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr5:94865200-94871600	Weak transcription	Colonic Mucosa	Colon
39	chr5:94865200-94875600	Weak transcription	Psoas Muscle	Psoas
40	chr5:94865200-94880200	Weak transcription	Spleen	Spleen
41	chr5:94865200-94889400	Weak transcription	Esophagus	oesophagus
42	chr5:94865200-94890000	Weak transcription	Aorta	Aorta
43	chr5:94865400-94871400	Weak transcription	Fetal Brain Female	brain
44	chr5:94865400-94872000	Weak transcription	A549	lung
45	chr5:94865400-94872200	Weak transcription	Brain Hippocampus Middle	brain
46	chr5:94865400-94875600	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr5:94865400-94875800	Weak transcription	Left Ventricle	heart
48	chr5:94865400-94876000	Weak transcription	HSMMtube	muscle
49	chr5:94865600-94871400	Weak transcription	HMEC	breast
50	chr5:94865800-94875600	Weak transcription	Fetal Brain Male	brain

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