Variant report
| Variant | nsv514785 |
|---|---|
| Chromosome Location | chr15:76341009-76346393 |
| allele | n/a |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:3)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:1 , 50 per page) page:
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| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr15:76341281..76343239-chr15:76349906..76351616,2 | MCF-7 | breast: |
(count:3 , 50 per page) page:
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| No. | lncRNA name | Chromosome Location | lncRNA alias |
|---|---|---|---|
| 1 | lnc-ETFA-2 | chr15:76344439-76344518 | NONHSAT047391 |
| 2 | lnc-ETFA-2 | chr15:76345580-76345710 | NONHSAT047391 |
| 3 | lnc-ETFA-2 | chr15:76345279-76345324 | NONHSAT047391 |
| No data |
| No data |
| No data |
Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page:
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| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs557394024 | chr15:76345302-76345303 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 2 | rs114139605 | chr15:76345600-76345601 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 3 | rs547000239 | chr15:76345601-76345602 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 4 | rs528068563 | chr15:76345677-76345678 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 5 | rs190260221 | chr15:76346258-76346259 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs548410628 | chr15:76346279-76346280 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs191463033 | chr15:76346287-76346288 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs570190633 | chr15:76346318-76346319 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs150310175 | chr15:76346319-76346320 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 10 | rs552844313 | chr15:76346379-76346380 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs571016407 | chr15:76346391-76346392 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:54)
| Disease | PMID | Source |
|---|---|---|
| Ewing''s sarcoma | 21437220 | CNVD |
| Schizophrenia | 19415332 | CNVD |
| Breast cancer | 22522925 | CNVD |
| Wilms tumour | 21544195 | CNVD |
| cataract | 16735990 | CNVD |
| Cancer | 21637783 | CNVD |
| Colorectal cancer | 20709793 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| spastic paraplegia with thinning of corpus callosum | 19105190 | CNVD |
| Schizophrenia | 21324950 | CNVD |
| Astrocytoma | 17387387 | CNVD |
| Esophageal squamous carcinoma | 21637470 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Disease | 21824424 | CNVD |
| Melanoma | 18172304 | CNVD |
| Gastric cancer | 17167181 | CNVD |
| Neuroblastoma | 19435921 | CNVD |
| Colorectal cancer | 19359472 | CNVD |
| Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
| Multiple myeloma | 17077331 | CNVD |
| Colorectal cancer | 16272173 | CNVD |
| Gastrointestinal stromal cancer | 20470368 | CNVD |
| Multiple myeloma | 17550852 | CNVD |
| Intellectual disability | 22102821 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Acute myeloid leukemia | 20729466 | CNVD |
| Basal cell lymphoma | 16317097 | CNVD |
| Diffuse large b-cell lymphoma | 16317097 | CNVD |
| Multiple myeloma | 20724749 | CNVD |
| Gastrointestinal stromal cancer | 16982739 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Basal cell lymphoma | 17170743 | CNVD |
| Follicular lymphoma | 17170743 | CNVD |
| Cancer | 16751803 | CNVD |
| Gastrointestinal stromal cancer | 20818650 | CNVD |
| Breast cancer | 17133270 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Acute promyelocytic leukemia | 19109227 | CNVD |
| Chronic lymphocytic leukemia | 21546498 | CNVD |
| Autism | 17322880 | CNVD |
| Acute lymphoblastic leukemia | 20067559 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Multiple myeloma | 16616336 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Congenital diaphragmatic hernia | 21085971 | CNVD |
| Papillary thyroid carcinoma | 22161024 | CNVD |
| Autism | 21480499 | CNVD |
| Breast cancer | 17603634 | CNVD |
| Acute myeloid leukemia | 16864856 | CNVD |
| Invasive pancreatic ductal carcinoma | 16982739 | CNVD |
| Breast cancer | 21364760 | CNVD |
| Pancreatic cancer | 17952125 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr15:76346200-76346400 | Enhancers | Hela-S3 | cervix |
