Variant report

Variant	nsv964086
Chromosome Location	chr4:119338967-119341856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 86 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:86 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144735430	chr4:119338968-119338969	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs185445160	chr4:119338974-119338975	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs528390995	chr4:119339045-119339046	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs535436855	chr4:119339058-119339059	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs370944618	chr4:119339133-119339134	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs188393653	chr4:119339166-119339167	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs541699182	chr4:119339181-119339182	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs1828857	chr4:119339182-119339183	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs1808022	chr4:119339208-119339209	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs556894418	chr4:119339222-119339223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1828856	chr4:119339227-119339228	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs530909226	chr4:119339336-119339337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs3896922	chr4:119339345-119339346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546352195	chr4:119339367-119339368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553393316	chr4:119339458-119339459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573320721	chr4:119339484-119339485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542246312	chr4:119339499-119339500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs4103597	chr4:119339515-119339516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs3879776	chr4:119339569-119339570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs71608371	chr4:119339691-119339692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531124020	chr4:119339767-119339768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544761463	chr4:119339913-119339914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564550691	chr4:119339923-119339924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532064782	chr4:119339950-119339951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4103612	chr4:119340054-119340055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565335863	chr4:119340062-119340063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570529012	chr4:119340064-119340065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528034062	chr4:119340077-119340078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533190988	chr4:119340139-119340140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574863506	chr4:119340163-119340164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181218832	chr4:119340164-119340165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4001535	chr4:119340192-119340193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568311096	chr4:119340203-119340204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4001536	chr4:119340269-119340270	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
35	rs536136800	chr4:119340287-119340288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549321029	chr4:119340318-119340319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569387784	chr4:119340321-119340322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557098596	chr4:119340399-119340400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570594333	chr4:119340403-119340404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200318414	chr4:119340470-119340471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs71608374	chr4:119340504-119340505	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs185721854	chr4:119340511-119340512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71608375	chr4:119340514-119340515	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs573383062	chr4:119340518-119340519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535811268	chr4:119340553-119340554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1843662	chr4:119340679-119340680	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs576989188	chr4:119340691-119340692	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs4001513	chr4:119340692-119340693	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs544615123	chr4:119340718-119340719	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs200844818	chr4:119340740-119340741	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Autism	19246517	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119337400-119339200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr4:119337600-119339400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr4:119338000-119339200	Enhancers	HMEC	breast
4	chr4:119338000-119339400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:119338000-119339400	Enhancers	NHEK	skin
6	chr4:119338400-119339000	Enhancers	HSMMtube	muscle
7	chr4:119338400-119339400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr4:119338600-119339000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:119338600-119339200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr4:119338600-119339200	Enhancers	Liver	Liver
11	chr4:119338600-119339800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:119338800-119339200	Bivalent Enhancer	Osteobl	bone
13	chr4:119339200-119339400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr4:119339200-119340600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr4:119340600-119340800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr4:119340600-119341000	Active TSS	Osteobl	bone
17	chr4:119340800-119345400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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