Variant report
Variant | esv1686486 |
---|---|
Chromosome Location | chr10:21615107-21615341 |
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 | rs375306698 | chr10:21615119-21615120 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
2 | rs375350095 | chr10:21615127-21615128 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
3 | rs572641051 | chr10:21615136-21615137 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
4 | rs369066090 | chr10:21615142-21615143 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
5 | rs367647428 | chr10:21615148-21615149 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs372604501 | chr10:21615153-21615154 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs192358689 | chr10:21615157-21615158 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs371816003 | chr10:21615163-21615164 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
9 | rs377224652 | chr10:21615189-21615190 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs554128714 | chr10:21615234-21615235 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
11 | rs532026431 | chr10:21615270-21615271 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
12 | rs532505496 | chr10:21615301-21615302 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs377235933 | chr10:21615328-21615329 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
14 | rs574373893 | chr10:21615330-21615331 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
15 | rs540317939 | chr10:21615339-21615340 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
16 | rs553623221 | chr10:21615341-21615342 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
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 |
Multiple myeloma | 16616336 | CNVD |
T-cell lymphomas | 19863542 | CNVD |
Esophageal cancer | 21851588 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Olfactory neuroblastoma | 18408657 | CNVD |
Breast cancer | 21364760 | CNVD |
Glioblastoma multiforme | 21525872 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:21607800-21615800 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
2 | chr10:21608000-21619000 | Weak transcription | Lung | lung |
3 | chr10:21608800-21615800 | Weak transcription | A549 | lung |
4 | chr10:21612800-21616000 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |