Variant report
Variant | esv3417435 |
---|---|
Chromosome Location | chr10:37644146-37650344 |
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)
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No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs568547655 | chr10:37646610-37646611 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
2 | rs7909101 | chr10:37646669-37646670 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
3 | rs13377062 | chr10:37646676-37646677 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
4 | rs565385939 | chr10:37646684-37646685 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
5 | rs374152030 | chr10:37646685-37646686 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
6 | rs182246682 | chr10:37646703-37646704 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
7 | rs371617277 | chr10:37646704-37646705 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
8 | rs552540480 | chr10:37646707-37646708 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
9 | rs566177940 | chr10:37646795-37646796 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
10 | rs535086805 | chr10:37646813-37646814 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
11 | rs555129387 | chr10:37646854-37646855 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
12 | rs367704791 | chr10:37646901-37646902 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
13 | rs575314768 | chr10:37646910-37646911 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
14 | rs367645798 | chr10:37646911-37646912 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
15 | rs377234859 | chr10:37646921-37646922 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
16 | rs537618139 | chr10:37646945-37646946 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
17 | rs370149343 | chr10:37646970-37646971 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
18 | rs184910809 | chr10:37646989-37646990 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
19 | rs190897720 | chr10:37646999-37647000 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
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 |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Breast cancer | 21858162 | CNVD |
Acute lymphoblastic leukemia | 20724749 | CNVD |
Autism | 22495311 | CNVD |
T-cell lymphomas | 19863542 | CNVD |
Esophageal cancer | 21851588 | CNVD |
Behavioral abnormalities | 21522184 | CNVD |
Dysmorphic features | 21522184 | CNVD |
Oral squamous cell carcinoma | 17134496 | CNVD |
Bethlem myopathy | 20302629 | CNVD |
Non-muscle invasive bladder neoplasm | 19445696 | CNVD |
Glioblastoma multiforme | 22286061 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Prostate cancer | 18632612 | CNVD |
Hepatocellular carcinoma | 16785998 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Barrett''s adenocarcinoma | 18663352 | CNVD |
Breast cancer | 21364760 | CNVD |
Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
Bipolar disorder | 19114987 | CNVD |
Breast cancer | 22522925 | CNVD |
Lung cancer | 21569311 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:37646600-37647000 | ZNF genes & repeats | Pancreas | Pancrea |