Variant report

Variant	rs74011718
Chromosome Location	chr15:40247278-40247279
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs17848500	1.00[AMR][1000 genomes]
rs56246581	0.81[AFR][1000 genomes]
rs59551980	0.81[AFR][1000 genomes]
rs61375261	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61490790	0.81[AFR][1000 genomes]
rs74009009	0.81[AFR][1000 genomes]
rs74009010	0.95[AFR][1000 genomes]
rs74009078	0.81[AFR][1000 genomes]
rs74009081	0.95[AFR][1000 genomes]
rs74011703	1.00[AMR][1000 genomes]
rs74011719	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74011721	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74011722	0.81[AFR][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	nsv530816	chr15:40003136-40586792	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	nsv832983	chr15:40098766-40248839	Genic enhancers Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40227200-40247800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:40227200-40248200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr15:40227200-40268400	Weak transcription	Esophagus	oesophagus
4	chr15:40227400-40283400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr15:40227800-40268400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:40228200-40323800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr15:40230000-40263000	Strong transcription	Fetal Muscle Trunk	muscle
8	chr15:40230200-40255600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr15:40230400-40261600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr15:40230600-40252400	Weak transcription	Right Atrium	heart
11	chr15:40231000-40268400	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr15:40231800-40252600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
13	chr15:40232000-40261400	Strong transcription	Skeletal Muscle Female	skeletal muscle
14	chr15:40232000-40262600	Strong transcription	Liver	Liver
15	chr15:40232200-40250200	Strong transcription	Sigmoid Colon	Sigmoid Colon
16	chr15:40232200-40252400	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr15:40232400-40252400	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr15:40232600-40251000	Strong transcription	Left Ventricle	heart
19	chr15:40232600-40251800	Strong transcription	Adipose Nuclei	Adipose
20	chr15:40233400-40248600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr15:40235000-40263000	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr15:40236000-40255400	Strong transcription	Fetal Lung	lung
23	chr15:40236000-40260000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr15:40236600-40303000	Weak transcription	Small Intestine	intestine
25	chr15:40237800-40255600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr15:40238000-40277800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr15:40238600-40268200	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr15:40238600-40272200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr15:40238800-40248600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr15:40238800-40273200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr15:40239200-40259600	Weak transcription	Fetal Brain Male	brain
32	chr15:40239400-40261200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr15:40239400-40262000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr15:40239600-40251400	Strong transcription	Osteobl	bone
35	chr15:40239600-40261400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr15:40239800-40262200	Strong transcription	Muscle Satellite Cultured Cells	--
37	chr15:40240000-40251200	Strong transcription	NHDF-Ad	bronchial
38	chr15:40240200-40261000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr15:40240400-40252000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr15:40240800-40268000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr15:40241000-40250200	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr15:40241000-40252400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr15:40241000-40252400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr15:40241000-40268600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr15:40241200-40249400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr15:40241200-40250000	Strong transcription	Fetal Intestine Small	intestine
47	chr15:40241200-40272600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr15:40241400-40256000	Strong transcription	Primary T cells from cord blood	blood
49	chr15:40241400-40260800	Strong transcription	Rectal Mucosa Donor 31	rectum
50	chr15:40241400-40262800	Strong transcription	Fetal Intestine Large	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links