Variant report
| Variant | esv2111417 |
|---|---|
| Chromosome Location | chr4:86238798-86239258 |
| 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 |
(count:1 , 50 per page) page:
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| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr4:86048857..86049411-chr4:86239183..86239916,2 | MCF-7 | breast: |
| No data |
| No data |
| No data |
| No data |
Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page:
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| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs571584354 | chr4:86238847-86238848 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 2 | rs199643307 | chr4:86238922-86238923 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 3 | rs537133045 | chr4:86238946-86238947 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs116120211 | chr4:86238954-86238955 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs11931292 | chr4:86238964-86238965 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 6 | rs79628384 | chr4:86238979-86238980 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs66483940 | chr4:86238980-86238981 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs11931323 | chr4:86239048-86239049 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs368781542 | chr4:86239058-86239059 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 10 | rs4423866 | chr4:86239068-86239069 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs572090677 | chr4:86239096-86239097 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs189270600 | chr4:86239118-86239119 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs377274211 | chr4:86239165-86239166 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 14 | rs138676966 | chr4:86239179-86239180 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 15 | rs567448068 | chr4:86239189-86239190 | Weak transcription | 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 |
| 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 |
| 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 |
| 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 |
| primary effusion lymphomas | 17116491 | CNVD |
| Prostate cancer | 16573809 | CNVD |
| Olfactory neuroblastoma | 18408657 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Splenic marginal zone lymphoma | 21957467 | CNVD |
| Breast cancer | 17133270 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Pancreatic cancer | 17952125 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr4:86237800-86238800 | Enhancers | Adipose Nuclei | Adipose |
| 2 | chr4:86238800-86239200 | Weak transcription | Adipose Nuclei | Adipose |
| 3 | chr4:86239200-86240200 | Enhancers | Adipose Nuclei | Adipose |
