Variant report

Variant	rs56056018
Chromosome Location	chr4:47455085-47455086
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs28493220	0.83[AMR][1000 genomes]
rs28525043	0.83[AMR][1000 genomes]
rs55696085	0.83[AMR][1000 genomes]
rs58507357	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs59324835	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs60727801	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6818323	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73813529	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73813530	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73813531	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73813540	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73813541	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73813543	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73813547	0.83[AMR][1000 genomes]
rs7684002	1.00[AFR][1000 genomes];0.83[AMR][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	nsv998919	chr4:47207023-47476876	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv879005	chr4:47408838-47548254	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv829923	chr4:47436139-47678443	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47436800-47465000	Weak transcription	Gastric	stomach
2	chr4:47438600-47464200	Weak transcription	Small Intestine	intestine
3	chr4:47441000-47456000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr4:47442200-47464000	Weak transcription	Left Ventricle	heart
5	chr4:47443600-47464000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:47445400-47465000	Weak transcription	Lung	lung
7	chr4:47445600-47464000	Weak transcription	Pancreas	Pancrea
8	chr4:47445600-47464200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr4:47445600-47464200	Weak transcription	Thymus	Thymus
10	chr4:47445800-47465000	Weak transcription	Aorta	Aorta
11	chr4:47446000-47465000	Weak transcription	Esophagus	oesophagus
12	chr4:47446600-47463000	Weak transcription	Brain Anterior Caudate	brain
13	chr4:47447000-47461400	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr4:47449600-47464200	Weak transcription	Fetal Brain Male	brain
15	chr4:47449800-47465000	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr4:47450600-47464400	Weak transcription	Brain Cingulate Gyrus	brain
17	chr4:47450600-47464600	Weak transcription	Rectal Smooth Muscle	rectum
18	chr4:47450600-47464800	Weak transcription	Colonic Mucosa	Colon
19	chr4:47450600-47464800	Weak transcription	A549	lung
20	chr4:47450800-47456000	Weak transcription	NHEK	skin
21	chr4:47450800-47463600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr4:47451000-47457200	Strong transcription	Primary T cells from cord blood	blood
23	chr4:47451000-47460800	Weak transcription	HMEC	breast
24	chr4:47451000-47464400	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr4:47451400-47456400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr4:47451400-47458800	Strong transcription	Osteobl	bone
27	chr4:47451400-47462400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr4:47451400-47464000	Weak transcription	Colon Smooth Muscle	Colon
29	chr4:47451800-47456200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr4:47451800-47456400	Strong transcription	Duodenum Smooth Muscle	Duodenum
31	chr4:47451800-47458200	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr4:47451800-47458200	Strong transcription	Dnd41	blood
33	chr4:47451800-47461800	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr4:47451800-47462200	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr4:47451800-47464600	Weak transcription	Hela-S3	cervix
36	chr4:47452000-47455600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:47452000-47456400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr4:47452000-47456600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr4:47452000-47456600	Strong transcription	Primary B cells from peripheral blood	blood
40	chr4:47452000-47456600	Strong transcription	Primary hematopoietic stem cells	blood
41	chr4:47452000-47456600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr4:47452000-47456600	Strong transcription	Placenta	Placenta
43	chr4:47452000-47458200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr4:47452000-47458200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr4:47452000-47459600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:47452000-47460200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr4:47452000-47461600	Strong transcription	Primary B cells from cord blood	blood
48	chr4:47452000-47464600	Weak transcription	K562	blood
49	chr4:47452200-47459400	Strong transcription	HSMM	muscle
50	chr4:47452400-47455800	Weak transcription	Fetal Lung	lung

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