Variant report
Variant | esv3435128 |
---|---|
Chromosome Location | chr10:118988554-118991767 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- 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 | rs528825509 | chr10:118991407-118991408 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
2 | rs185426882 | chr10:118991420-118991421 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
3 | rs555410876 | chr10:118991424-118991425 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
4 | rs568913602 | chr10:118991438-118991439 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
5 | rs111944165 | chr10:118991440-118991441 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
6 | rs370614760 | chr10:118991501-118991502 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
7 | rs551546202 | chr10:118991503-118991504 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
8 | rs115384584 | chr10:118991521-118991522 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
9 | rs534085927 | chr10:118991533-118991534 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
10 | rs74159130 | chr10:118991550-118991551 | Active TSS | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
11 | rs367779208 | chr10:118991552-118991553 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
12 | rs363329 | chr10:118991582-118991583 | Active TSS | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
13 | rs375596499 | chr10:118991615-118991616 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
14 | rs138231154 | chr10:118991653-118991654 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
15 | rs2532799 | chr10:118991695-118991696 | Active TSS | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
16 | rs12414893 | chr10:118991727-118991728 | Active TSS | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
17 | rs572276210 | chr10:118991728-118991729 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Gastric cancer | 17908304 | CNVD |
Chordoma | 21602918 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Melanoma | 18172304 | CNVD |
Pleomorphic xanthoastrocytoma | 20730472 | CNVD |
Ewing''s sarcoma | 17952124 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Acute lymphoblastic leukemia | 20724749 | CNVD |
Prostate cancer | 18632612 | CNVD |
Cockayne syndrome | 18421352 | CNVD |
Glioblastoma | 16823260 | CNVD |
Medulloblastoma | 16968546 | CNVD |
Neuroblastoma | 17533364 | CNVD |
Squamous cell cancer | 21044232 | CNVD |
Glioma | 21971842 | CNVD |
Cancer | 21637783 | CNVD |
Non-small cell lung cancer | 21044232 | CNVD |
Non-syndromic sensorineural hearing loss | 18471307 | CNVD |
Colorectal cancer | 20709793 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Breast cancer | 21264507 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Liposarcoma | 21253554 | CNVD |
Oligodendroglial tumors | 17285580 | CNVD |
Lung cancer | 18438408 | CNVD |
Medulloblastoma | 16783165 | CNVD |
Breast cancer | 21785460 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Paraganglioma | 17535989 | CNVD |
Gastrointestinal stromal cancer | 17535989 | CNVD |
Pancreatic endocrine tumor | 17639061 | CNVD |
Pulmonary chondroma | 17535989 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 17603634 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Wilms tumour | 21544195 | CNVD |
Prostate cancer | 16573809 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Breast cancer | 16608533 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Glioblastoma multiforme | 17002787 | CNVD |
Breast cancer | 17393978 | CNVD |
Ovarian cancer | 21720365 | CNVD |
Splenic marginal zone lymphoma | 21957467 | CNVD |
Cornelia de Lange syndrome | 24599119 | CNVD |
T-cell lymphomas | 19863542 | CNVD |
Breast cancer | 16397240 | CNVD |
Urothelial carcinoma | 21177765 | CNVD |
Chronic lymphocytic leukemia | 18645599 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Barrett''s syndrome | 19417022 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Breast cancer | 21364760 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Glioblastoma multiforme | 22286061 | CNVD |
Barrett''s adenocarcinoma | 18663352 | CNVD |
Neuroticism | 17667963 | CNVD |
Malignant fibrous histiocytomas | 21085701 | CNVD |
Myxofibrosarcoma | 16751306 | CNVD |
Breast cancer | 17133270 | CNVD |
Breast cancer | 21509527 | CNVD |
Sezary syndrome | 18413736 | CNVD |
Pancreatic cancer | 17952125 | CNVD |
Breast cancer | 22522925 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:118991400-118992200 | Active TSS | Spleen | Spleen |