Variant report
| Variant | esv3356188 |
|---|---|
| Chromosome Location | chr20:26073152-26077450 |
| allele | n/a |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
| No data |
(count:1 , 50 per page) page:
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| No. | lncRNA name | Chromosome Location | lncRNA alias |
|---|---|---|---|
| 1 | lnc-FAM182A-4 | chr20:26073445-26073683 | ENSG00000125804.9 |
| No data |
| No data |
| No data |
Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs570241868 | chr20:26073457-26073458 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 2 | rs6132919 | chr20:26073480-26073481 | Inactive region | lncRNA | n/a | Overlapped CNVs | mRNA abundance |
| 3 | rs559148712 | chr20:26073485-26073486 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 4 | rs79462922 | chr20:26073487-26073488 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 5 | rs75192218 | chr20:26073516-26073517 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 6 | rs374700437 | chr20:26073526-26073527 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 7 | rs6115516 | chr20:26073561-26073562 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 8 | rs544895065 | chr20:26073580-26073581 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 9 | rs564534151 | chr20:26073589-26073590 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 10 | rs2996701 | chr20:26073621-26073622 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 11 | rs367839590 | chr20:26073639-26073640 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 12 | rs554939325 | chr20:26073645-26073646 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 13 | rs397835052 | chr20:26073652-26073653 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 14 | rs75345480 | chr20:26073653-26073654 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 15 | rs540657155 | chr20:26073670-26073671 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 16 | rs201391122 | chr20:26073674-26073675 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:43)
| Disease | PMID | Source |
|---|---|---|
| Cancer | 21637783 | CNVD |
| Non-syndromic sensorineural hearing loss | 18471307 | CNVD |
| Esophageal squamous carcinoma | 21637470 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Oral cancer | 19627613 | CNVD |
| colon cancer | 17210682 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Thyroid cancer | 19087340 | CNVD |
| Acute lymphoblastic leukemia | 20067559 | CNVD |
| Cancer | 16751803 | CNVD |
| Chronic lymphocytic leukemia | 21546498 | CNVD |
| Colorectal cancer | 19359472 | CNVD |
| Esophageal squamous carcinoma | 18350619 | CNVD |
| Human rectal carcinomas | 16397240 | CNVD |
| Olfactory neuroblastoma | 18408657 | CNVD |
| Central neurocytomas | 17123091 | CNVD |
| Colorectal cancer | 16272173 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| Gastric cancer | 17908304 | CNVD |
| Urothelial carcinoma | 21177765 | CNVD |
| Acute myeloid leukemia | 20729466 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Ewing''s sarcoma | 17952124 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Thoracic aortic aneurysm | 21092924 | CNVD |
| Colorectal cancer | 21645411 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Autism | 22495311 | CNVD |
| Anaplastic large cell lymphoma | 18179710 | CNVD |
| T-cell prolymphocytic leukemia | 17713554 | CNVD |
| Cancer | 21183584 | CNVD |
| Myxofibrosarcoma | 16751306 | CNVD |
| Pancreatic endocrine tumor | 17639061 | CNVD |
| Esophageal cancer | 21851588 | CNVD |
| Chordoma | 18071362 | CNVD |
| Basal cell lymphoma | 16317097 | CNVD |
| Diffuse large b-cell lymphoma | 16317097 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Colorectal cancer | 16774939 | CNVD |
| Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
| Congenital anomalies of the kidney and urinary tract | 18316590 | CNVD |
Chromatin state (count:0 , 50 per page) page:
| No data |
