Variant report
Variant | nsv594707 |
---|---|
Chromosome Location | chr4:80353066-80362657 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr4:80349558..80352426-chr4:80355667..80358007,3 | K562 | blood: |
No data |
No data |
No data |
No data |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs12645140 | chr4:80353066-80353067 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
2 | rs567031115 | chr4:80353109-80353110 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
3 | rs532776589 | chr4:80353136-80353137 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
4 | rs146878888 | chr4:80353182-80353183 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs569406333 | chr4:80353239-80353240 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
6 | rs538346650 | chr4:80353256-80353257 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs185791666 | chr4:80353262-80353263 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs568509450 | chr4:80353268-80353269 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs534184514 | chr4:80353285-80353286 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
10 | rs190988011 | chr4:80353304-80353305 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs35797196 | chr4:80353318-80353319 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs112894686 | chr4:80353334-80353335 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs183126892 | chr4:80353335-80353336 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs538894491 | chr4:80353346-80353347 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs35049153 | chr4:80353359-80353360 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs558473580 | chr4:80353366-80353367 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs140694917 | chr4:80353400-80353401 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
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 |
lymphocytic leukemia | 21291569 | 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 |
Glioblastoma multiforme | 21922591 | CNVD |
Parkinson disease | 21956041 | CNVD |
Mental retardation | 20522426 | CNVD |
delayed speech | 20522426 | CNVD |
growth disorder | 20522426 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Myxofibrosarcoma | 16751306 | CNVD |
Esophageal squamous carcinoma | 18350619 | CNVD |
Parkinson disease | 18923514 | CNVD |
Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
Cancer | 21183584 | 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 |
Basal cell lymphoma | 17170743 | CNVD |
Follicular lymphoma | 17170743 | CNVD |
Chronic lymphocytic leukemia | 20421269 | CNVD |
Myelodysplastic syndrome | 21251322 | CNVD |
Multiple myeloma | 17550852 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Lung cancer | 18438408 | CNVD |
Chronic lymphocytic leukemia | 18922857 | CNVD |
Cancer | 22429812 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Autism | 18414403 | CNVD |
Chronic lymphocytic leukemia | 21670202 | CNVD |
primary effusion lymphomas | 17116491 | CNVD |
Gastric cancer | 16891809 | CNVD |
Prostate cancer | 16573809 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Neuroblastoma | 21899760 | CNVD |
Non-syndromic sensorineural hearing loss | 21987784 | CNVD |
Myelodysplastic syndrome | 18508791 | CNVD |
Cancer | 22183965 | CNVD |
Melanoma | 22183965 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:80353000-80353200 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
2 | chr4:80353000-80353400 | Enhancers | Adipose Nuclei | Adipose |
3 | chr4:80353000-80353400 | Enhancers | Fetal Heart | heart |
4 | chr4:80353000-80353400 | Enhancers | Fetal Muscle Leg | muscle |
5 | chr4:80353200-80353400 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |