Variant report
| Variant | esv3501701 |
|---|---|
| Chromosome Location | chr2:188059701-188062143 |
| allele | n/a |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:1 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr2:188049075..188051640-chr2:188058153..188060182,2 | K562 | blood: |
(count:1 , 50 per page) page:
1
| No. | lncRNA name | Chromosome Location | lncRNA alias |
|---|---|---|---|
| 1 | lnc-FAM171B-1 | chr2:188060089-188060574 | NONHSAT076011 |
| No data |
| No data |
| No data |
Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs528548293 | chr2:188060096-188060097 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 2 | rs565017697 | chr2:188060104-188060105 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 3 | rs76493184 | chr2:188060123-188060124 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 4 | rs531877693 | chr2:188060148-188060149 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 5 | rs543439901 | chr2:188060157-188060158 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 6 | rs565242585 | chr2:188060176-188060177 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 7 | rs569249521 | chr2:188060201-188060202 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 8 | rs75084966 | chr2:188060202-188060203 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 9 | rs367946335 | chr2:188060237-188060238 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 10 | rs548663822 | chr2:188060240-188060241 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 11 | rs78009609 | chr2:188060273-188060274 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 12 | rs72904948 | chr2:188060414-188060415 | Inactive region | lncRNA | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 13 | rs200588779 | chr2:188060430-188060431 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 14 | rs11675409 | chr2:188060444-188060445 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 15 | rs373639082 | chr2:188060466-188060467 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 16 | rs116001535 | chr2:188060468-188060469 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 17 | rs73979701 | chr2:188060494-188060495 | Inactive region | lncRNA | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 18 | rs537986702 | chr2:188060519-188060520 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:52)
| Disease | PMID | Source |
|---|---|---|
| Breast cancer | 17603634 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| Ependymoma | 16718352 | CNVD |
| Thoracic aortic aneurysm | 21092924 | CNVD |
| Intellectual disability | 22102821 | CNVD |
| Melanoma | 18172304 | CNVD |
| Cancer | 16751803 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Acute lymphoblastic leukemia | 20067559 | CNVD |
| Acute lymphoblastic leukemia | 21980252 | CNVD |
| Testicular germ cell tumor | 18059402 | CNVD |
| Breast cancer | 16272173 | CNVD |
| Ewing''s sarcoma | 17952124 | 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 |
| Colorectal cancer | 16272173 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Glioblastoma | 21080181 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| Acute myeloid leukemia | 20729466 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Facial dysmorphism | 20548289 | CNVD |
| Mental retardation | 20548289 | CNVD |
| Biliary cancer | 20360734 | CNVD |
| Breast cancer | 20360734 | CNVD |
| Coronary artery disease | 20360734 | CNVD |
| Crohn''s disease | 20360734 | CNVD |
| Hypertension | 20360734 | CNVD |
| Rheumatoid arthritis | 20360734 | CNVD |
| Type 1 diabetes | 20360734 | CNVD |
| Type 2 diabetes | 20360734 | CNVD |
| Breast cancer | 21364760 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Hirschsprung''s Disease | 21712996 | CNVD |
| Cancer | 21183584 | CNVD |
| Sudden cardiac death | 19188705 | CNVD |
| Autism | 19329560 | CNVD |
| Urothelial carcinoma | 21177765 | CNVD |
| early-passage human iPS cells | 21368824 | CNVD |
| Pancreatic cancer | 17952125 | CNVD |
| Breast cancer | 22522925 | CNVD |
| Cancer | 20164919 | CNVD |
Chromatin state (count:0 , 50 per page) page:
| No data |
