Variant report
| Variant | esv3498366 |
|---|---|
| Chromosome Location | chr15:55217610-55225608 |
| allele | n/a |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
| No data |
| No data |
| No data |
| No data |
| No data |
Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs184188326 | chr15:55225209-55225210 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 2 | rs72738252 | chr15:55225213-55225214 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 3 | rs188131540 | chr15:55225217-55225218 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs543351094 | chr15:55225223-55225224 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs556569893 | chr15:55225291-55225292 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs576412034 | chr15:55225344-55225345 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs181037993 | chr15:55225404-55225405 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs565246216 | chr15:55225430-55225431 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs78233739 | chr15:55225443-55225444 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 10 | rs187381856 | chr15:55225455-55225456 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs560344667 | chr15:55225467-55225468 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs577322112 | chr15:55225518-55225519 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs34284889 | chr15:55225535-55225536 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 14 | rs529071532 | chr15:55225549-55225550 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 15 | rs140341386 | chr15:55225563-55225564 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 16 | rs192063041 | chr15:55225570-55225571 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 17 | rs531471379 | chr15:55225587-55225588 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 18 | rs181780930 | chr15:55225590-55225591 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 19 | rs570867867 | chr15:55225592-55225593 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 20 | rs111412147 | chr15:55225598-55225599 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:67)
| Disease | PMID | Source |
|---|---|---|
| Ewing''s sarcoma | 21437220 | CNVD |
| Schizophrenia | 19415332 | CNVD |
| Breast cancer | 22522925 | CNVD |
| Autism | 22495311 | CNVD |
| Wilms tumour | 21544195 | CNVD |
| Testicular germ cell tumor | 18059402 | CNVD |
| cataract | 16735990 | CNVD |
| Cancer | 21637783 | CNVD |
| Colorectal cancer | 20709793 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| spastic paraplegia with thinning of corpus callosum | 19105190 | CNVD |
| Schizophrenia | 21324950 | CNVD |
| Astrocytoma | 17387387 | CNVD |
| Esophageal squamous carcinoma | 21637470 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Disease | 21824424 | CNVD |
| Melanoma | 18172304 | CNVD |
| Colorectal cancer | 16774939 | CNVD |
| Gastric cancer | 17167181 | CNVD |
| Neuroblastoma | 19435921 | CNVD |
| Colorectal cancer | 19359472 | CNVD |
| Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
| Multiple myeloma | 17077331 | CNVD |
| Colorectal cancer | 16272173 | CNVD |
| Gastrointestinal stromal cancer | 20470368 | CNVD |
| Multiple myeloma | 17550852 | CNVD |
| Intellectual disability | 22102821 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Acute myeloid leukemia | 20729466 | CNVD |
| Prostate cancer | 16573809 | CNVD |
| Basal cell lymphoma | 16317097 | CNVD |
| Diffuse large b-cell lymphoma | 16317097 | CNVD |
| Multiple myeloma | 20724749 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Chronic lymphocytic leukemia | 21546498 | CNVD |
| Gastrointestinal stromal cancer | 16982739 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Basal cell lymphoma | 17053054 | CNVD |
| Breast cancer | 22032731 | CNVD |
| Basal cell lymphoma | 17170743 | CNVD |
| Follicular lymphoma | 17170743 | CNVD |
| Hirschsprung''s Disease | 21712996 | CNVD |
| Myeloproliferative neoplasm | 20015882 | CNVD |
| Cancer | 21129771 | CNVD |
| Breast cancer | 16272173 | CNVD |
| Hepatocellular carcinoma | 16750200 | CNVD |
| Abnormal phenotypes | 18644119 | CNVD |
| Cancer | 16751803 | CNVD |
| Esophageal adenocarcinoma | 18820669 | CNVD |
| Gastrointestinal stromal cancer | 20818650 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Acute monocytic leukemia | 16498392 | CNVD |
| Oral squamous cell carcinoma | 17134496 | CNVD |
| Breast cancer | 17133270 | CNVD |
| Urothelial carcinoma | 21177765 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Cancer | 17440070 | CNVD |
| Breast cancer | 20668451 | CNVD |
| Cancer | 20668451 | CNVD |
| Lung cancer | 20668451 | CNVD |
| Ovarian cancer | 20668451 | CNVD |
| Pancreas cancer | 20668451 | CNVD |
| Prostate cancer | 20668451 | CNVD |
| Pancreatic cancer | 17952125 | CNVD |
| Cancer | 20164919 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr15:55225200-55252800 | Weak transcription | Aorta | Aorta |
