Variant report
Variant | esv3486976 |
---|---|
Chromosome Location | chr10:19397265-19397694 |
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 |
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No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs537784673 | chr10:19397308-19397309 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
2 | rs375515825 | chr10:19397316-19397317 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
3 | rs11008504 | chr10:19397318-19397319 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
4 | rs147260219 | chr10:19397319-19397320 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
5 | rs139267490 | chr10:19397324-19397325 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs35948766 | chr10:19397354-19397355 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs61851286 | chr10:19397357-19397358 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs568092097 | chr10:19397404-19397405 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
9 | rs537020151 | chr10:19397412-19397413 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs201274655 | chr10:19397468-19397469 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
11 | rs372006890 | chr10:19397469-19397470 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
12 | rs370548981 | chr10:19397520-19397521 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs555662147 | chr10:19397593-19397594 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
14 | rs548761034 | chr10:19397598-19397599 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
15 | rs573871240 | chr10:19397636-19397637 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
16 | rs567124807 | chr10:19397637-19397638 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
17 | rs552607902 | chr10:19397641-19397642 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
18 | rs12221192 | chr10:19397655-19397656 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Medulloblastoma | 16783165 | CNVD |
Breast cancer | 17133270 | 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 |
Melanoma | 18172304 | CNVD |
Pleomorphic xanthoastrocytoma | 20730472 | CNVD |
Lung cancer | 18438408 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Ewing''s sarcoma | 17952124 | CNVD |
Oral cancer | 21386901 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Breast cancer | 21858162 | CNVD |
Acute lymphoblastic leukemia | 20724749 | CNVD |
Autism | 22495311 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Intracranial aneurysm | 16715129 | CNVD |
Cutaneous T-cell lymphoma | 21881587 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Multiple myeloma | 16616336 | CNVD |
T-cell lymphomas | 19863542 | CNVD |
Esophageal cancer | 21851588 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Epilepsy | 22083797 | CNVD |
Olfactory neuroblastoma | 18408657 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Breast cancer | 21364760 | CNVD |
Non-syndromic sensorineural hearing loss | 21293372 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:19392600-19398000 | Weak transcription | Fetal Intestine Small | intestine |
2 | chr10:19393200-19398000 | Weak transcription | Duodenum Mucosa | Duodenum |