Variant report
| Variant | esv1631254 |
|---|---|
| Chromosome Location | chr10:1743377-1743799 |
| 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:22 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs187341823 | chr10:1743405-1743406 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 2 | rs368145324 | chr10:1743450-1743451 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 3 | rs371614490 | chr10:1743452-1743453 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs113800091 | chr10:1743476-1743477 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs112329323 | chr10:1743503-1743504 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs375175432 | chr10:1743519-1743520 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs368249348 | chr10:1743531-1743532 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs372836263 | chr10:1743603-1743604 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs375768556 | chr10:1743611-1743612 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 10 | rs77619529 | chr10:1743629-1743630 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs371773756 | chr10:1743671-1743672 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs374352098 | chr10:1743700-1743701 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs562770704 | chr10:1743710-1743711 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 14 | rs74775971 | chr10:1743715-1743716 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 15 | rs376551642 | chr10:1743731-1743732 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 16 | rs56326508 | chr10:1743733-1743734 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 17 | rs531418056 | chr10:1743739-1743740 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 18 | rs74660836 | chr10:1743757-1743758 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 19 | rs7072134 | chr10:1743773-1743774 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 20 | rs74838696 | chr10:1743788-1743789 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 21 | rs75241548 | chr10:1743790-1743791 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 22 | rs547451706 | chr10:1743799-1743800 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:56)
| Disease | PMID | Source |
|---|---|---|
| Myelofibrosis | 22110671 | CNVD |
| Breast cancer | 20409316 | CNVD |
| Gastric adenocarcinoma | 19115996 | CNVD |
| Pilocytic astrocytoma | 18622384 | CNVD |
| Pilomyxoid astrocytoma | 18622384 | CNVD |
| Breast cancer | 17133270 | CNVD |
| T-cell acute lymphoblastic leukemia | 18185524 | CNVD |
| Cancer | 21129771 | CNVD |
| Sudden cardiac death | 19188705 | CNVD |
| Digeorge syndrome | 22283845 | CNVD |
| Colorectal cancer | 20709793 | CNVD |
| Wilms tumour | 19047088 | CNVD |
| Hepatocellular carcinoma | 16750200 | CNVD |
| Acute myeloid leukemia | 16864856 | CNVD |
| Cancer | 21183584 | CNVD |
| Barakat syndrome | 22470819 | CNVD |
| Melanoma | 18172304 | CNVD |
| Ovarian cancer | 21720365 | CNVD |
| Autism | 18414403 | CNVD |
| Malignant melanoma | 18718029 | CNVD |
| Breast cancer | 22032731 | CNVD |
| Medulloblastoma | 16783165 | CNVD |
| Endometrioid adenocarcinoma | 16974079 | CNVD |
| Breast cancer | 17603634 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Esophageal squamous carcinoma | 21637470 | CNVD |
| Phyllodes tumor | 17334353 | CNVD |
| Acute lymphoblastic leukemia | 17690704 | CNVD |
| Pancreatic endocrine tumor | 17639061 | CNVD |
| Gastric cancer | 17908304 | CNVD |
| Chordoma | 21602918 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| Pleomorphic xanthoastrocytoma | 20730472 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Thoracic aortic aneurysm | 21092924 | CNVD |
| Melanoma | 17363583 | CNVD |
| low-grade B-cell lymphoma tumor | 18367492 | CNVD |
| Ewing''s sarcoma | 17952124 | CNVD |
| Oral cancer | 21386901 | CNVD |
| Breast cancer | 21785460 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Acute lymphoblastic leukemia | 20435627 | CNVD |
| Breast cancer | 21509527 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Breast cancer | 21858162 | CNVD |
| Breast cancer | 21364760 | CNVD |
| Acute lymphoblastic leukemia | 20724749 | CNVD |
| Autism | 22495311 | CNVD |
| Autism | 22543975 | CNVD |
| Breast cancer | 22522925 | CNVD |
| Pancreatic cancer | 17952125 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr10:1743400-1751000 | Weak transcription | Fetal Brain Male | brain |
