Variant report
Variant | esv3370355 |
---|---|
Chromosome Location | chr10:26259802-26260075 |
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 | rs578146665 | chr10:26259810-26259811 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
2 | rs11014880 | chr10:26259816-26259817 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
3 | rs557271162 | chr10:26259833-26259834 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
4 | rs192050470 | chr10:26259848-26259849 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
5 | rs542641637 | chr10:26259866-26259867 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs544354591 | chr10:26259891-26259892 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs544743465 | chr10:26259907-26259908 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs559406528 | chr10:26259945-26259946 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
9 | rs528601956 | chr10:26259993-26259994 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs140402932 | chr10:26260000-26260001 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
11 | rs370129370 | chr10:26260027-26260028 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
12 | rs143957427 | chr10:26260032-26260033 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs565095731 | chr10:26260040-26260041 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
14 | rs530678915 | chr10:26260058-26260059 | 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 |
T-cell lymphomas | 19863542 | CNVD |
Esophageal cancer | 21851588 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Behavioral abnormalities | 21522184 | CNVD |
Dysmorphic features | 21522184 | CNVD |
low-grade B-cell lymphoma tumor | 18367492 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Autism | 21439084 | CNVD |
Maculopathy | 20981449 | CNVD |
Ovine squamous-cell carcinoma | 17599052 | CNVD |
T-cell acute lymphoblastic leukemia | 18185524 | CNVD |
Oral squamous cell carcinoma | 17134496 | CNVD |
Glioblastoma multiforme | 21525872 | CNVD |
Adrenocortical carcinoma | 18281524 | CNVD |
Breast cancer | 21364760 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:26250800-26261200 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
2 | chr10:26254800-26270200 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
3 | chr10:26255000-26263200 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
4 | chr10:26255800-26263800 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
5 | chr10:26256400-26261400 | Weak transcription | Brain Germinal Matrix | brain |