Variant report
| Variant | esv3388678 |
|---|---|
| Chromosome Location | chr2:98078883-98082281 |
| allele | n/a |
| Outlinks | Ensembl UCSC |
- TF binding region (count:9)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:16)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:9 , 50 per page) page:
1
| No data |
| No data |
(count:16 , 50 per page) page:
1
| No. | lncRNA name | Chromosome Location | lncRNA alias |
|---|---|---|---|
| 1 | lnc-ACTR1B-3 | chr2:98081676-98082014 | NR_040097 |
| 2 | lnc-ACTR1B-3 | chr2:98081774-98082014 | ENSG00000230606.6 |
| 3 | lnc-ACTR1B-3 | chr2:98081774-98082014 | ENSG00000230606 |
| 4 | lnc-ACTR1B-3 | chr2:98081798-98082014 | ENSG00000230606.6 |
| 5 | lnc-ACTR1B-3 | chr2:98081774-98082014 | ENSG00000230606.6 |
| 6 | lnc-ACTR1B-3 | chr2:98081676-98082014 | NONHSAT072631 |
| 7 | lnc-ACTR1B-3 | chr2:98081928-98082014 | NONHSAT072638 |
| 8 | lnc-ACTR1B-3 | chr2:98081812-98082014 | ENSG00000230606.6 |
| 9 | lnc-ACTR1B-3 | chr2:98081922-98082014 | ENSG00000230606.6 |
| 10 | lnc-ACTR1B-3 | chr2:98081676-98082014 | NONHSAT072632 |
| 11 | lnc-ACTR1B-3 | chr2:98081683-98082014 | ENSG00000230606 |
| 12 | lnc-ACTR1B-3 | chr2:98081833-98082014 | ENSG00000230606.6 |
| 13 | lnc-ACTR1B-3 | chr2:98081083-98082014 | ENSG00000230606.6 |
| 14 | lnc-ACTR1B-3 | chr2:98081839-98082014 | ENSG00000230606.6 |
| 15 | lnc-ACTR1B-3 | chr2:98081851-98082014 | ENSG00000230606.6 |
| 16 | lnc-ACTR1B-3 | chr2:98081851-98082014 | NONHSAT072636 |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000241481 | TF binding region |
Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs4095720 | chr2:98081412-98081413 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 2 | rs569262667 | chr2:98081451-98081452 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 3 | rs558804438 | chr2:98081657-98081658 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:52)
| Disease | PMID | Source |
|---|---|---|
| Medulloblastoma | 21979893 | CNVD |
| Breast cancer | 17603634 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Ependymoma | 16718352 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| Thoracic aortic aneurysm | 21092924 | CNVD |
| Intellectual disability | 22102821 | CNVD |
| Cancer | 20164919 | CNVD |
| Autism | 17483303 | CNVD |
| Medulloblastoma | 20607354 | CNVD |
| Autism | 22495311 | CNVD |
| Autism | 18522746 | CNVD |
| Neurodevelopmental disorder | 22521361 | CNVD |
| Melanoma | 18172304 | CNVD |
| Cancer | 16751803 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Acute lymphoblastic leukemia | 20067559 | CNVD |
| Acute lymphoblastic leukemia | 21980252 | CNVD |
| Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
| Seminomas | 18059402 | CNVD |
| Testicular germ cell tumor | 18059402 | CNVD |
| Myxofibrosarcoma | 16751306 | CNVD |
| Breast cancer | 16272173 | CNVD |
| Ovarian cancer | 21781307 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Mowat-Wilson syndrome | 21572526 | CNVD |
| Disorders of sex development | 21048976 | CNVD |
| epilepsy | 18472482 | CNVD |
| Ewing''s sarcoma | 17952124 | CNVD |
| Hepatocellular carcinoma | 16750200 | CNVD |
| Cancer | 21637783 | CNVD |
| Non-syndromic sensorineural hearing loss | 18471307 | CNVD |
| Esophageal squamous carcinoma | 21637470 | CNVD |
| Liposarcoma | 21253554 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Embryonal rhabdomyosarcoma | 16790082 | CNVD |
| Autism | 16446308 | CNVD |
| Autism | 19401682 | CNVD |
| lymphocytic leukemia | 21291569 | CNVD |
| Breast cancer | 21509527 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Ovarian clear cell carcinoma | 19293255 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Intellectual disability | 22045946 | CNVD |
| Acute lymphoblastic leukemia | 18458336 | CNVD |
| Glioblastoma multiforme | 21138945 | CNVD |
| Malignant peripheral nerve sheath tumor | 18522746 | CNVD |
| Chronic lymphocytic leukemia | 21546498 | CNVD |
| Tetralogy of Fallot | 22912587 | CNVD |
| Breast cancer | 22522925 | CNVD |
Chromatin state (count:0 , 50 per page) page:
| No data |
