Variant report
| Variant | esv2086934 |
|---|---|
| Chromosome Location | chr10:61365303-61365983 |
| 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:13 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs16913829 | chr10:61365306-61365307 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 2 | rs541290736 | chr10:61365310-61365311 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 3 | rs183664755 | chr10:61365318-61365319 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs11815865 | chr10:61365321-61365322 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs575026357 | chr10:61365349-61365350 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs542350254 | chr10:61365357-61365358 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs572997544 | chr10:61365358-61365359 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs186504871 | chr10:61365376-61365377 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs373402676 | chr10:61365421-61365422 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 10 | rs530948433 | chr10:61365837-61365838 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs370612883 | chr10:61365885-61365886 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs541596670 | chr10:61365913-61365914 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs565069887 | chr10:61365942-61365943 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:59)
| Disease | PMID | Source |
|---|---|---|
| Pancreatic endocrine tumor | 17639061 | CNVD |
| Gastric cancer | 17908304 | CNVD |
| Chordoma | 21602918 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| Melanoma | 18172304 | CNVD |
| Pleomorphic xanthoastrocytoma | 20730472 | CNVD |
| Thoracic aortic aneurysm | 21092924 | CNVD |
| Ewing''s sarcoma | 17952124 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Acute lymphoblastic leukemia | 20435627 | CNVD |
| Acute lymphoblastic leukemia | 20724749 | CNVD |
| Autism | 22495311 | CNVD |
| Esophageal cancer | 21851588 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| Cockayne syndrome | 18421352 | CNVD |
| Glioblastoma | 16823260 | CNVD |
| Medulloblastoma | 16968546 | CNVD |
| Neuroblastoma | 17533364 | CNVD |
| T-cell lymphomas | 19863542 | CNVD |
| Testicular germ cell tumor | 18059402 | CNVD |
| Squamous cell cancer | 21044232 | CNVD |
| Glioma | 21971842 | CNVD |
| Cancer | 21637783 | CNVD |
| Non-small cell lung cancer | 21044232 | CNVD |
| Non-syndromic sensorineural hearing loss | 18471307 | CNVD |
| Colorectal cancer | 20709793 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Esophageal squamous carcinoma | 21637470 | CNVD |
| Liposarcoma | 21253554 | CNVD |
| Oligodendroglial tumors | 17285580 | CNVD |
| Obesity | 21956041 | CNVD |
| Basal cell lymphoma | 16317097 | CNVD |
| Diffuse large b-cell lymphoma | 16317097 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Breast cancer | 21364760 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Metanephric adenoma | 20802469 | CNVD |
| Autism | 20841430 | CNVD |
| Prostate cancer | 16573809 | CNVD |
| Schizophrenia | 19329560 | CNVD |
| Heart failure | 18772530 | CNVD |
| Heart failure | 18854381 | CNVD |
| Hyperglycemia | 19060297 | CNVD |
| Endometrioid adenocarcinoma | 16974079 | CNVD |
| Myeloproliferative neoplasm | 20015882 | CNVD |
| Usher syndrome | 20538994 | CNVD |
| Glioblastoma multiforme | 17002787 | CNVD |
| Urothelial carcinoma | 21177765 | CNVD |
| abnormal development | 18461090 | CNVD |
| Breast cancer | 21785460 | CNVD |
| Medulloblastoma | 16783165 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Epilepsy | 20643615 | CNVD |
| Neurodevelopmental disorder | 22521361 | CNVD |
| Breast cancer | 21509527 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr10:61355600-61366800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 2 | chr10:61362000-61368600 | Weak transcription | Placenta | Placenta |
