Variant report
| Variant | esv14931 |
|---|---|
| Chromosome Location | chr11:8200989-8201455 |
| allele | n/a |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- 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 | chr11:8191876..8193485-chr11:8198068..8201621,3 | K562 | blood: |
| No data |
| No data |
| No data |
| No data |
Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs75001724 | chr11:8201038-8201039 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 2 | rs117622952 | chr11:8201044-8201045 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 3 | rs374651064 | chr11:8201057-8201058 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs371842537 | chr11:8201060-8201061 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs537469123 | chr11:8201081-8201082 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs7481667 | chr11:8201125-8201126 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 7 | rs146762138 | chr11:8201159-8201160 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs577390937 | chr11:8201185-8201186 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs7481683 | chr11:8201186-8201187 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 10 | rs539946801 | chr11:8201193-8201194 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs560312063 | chr11:8201269-8201270 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs374427188 | chr11:8201279-8201280 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs7479133 | chr11:8201305-8201306 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 14 | rs141162667 | chr11:8201325-8201326 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 15 | rs563070695 | chr11:8201349-8201350 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 16 | rs7479738 | chr11:8201355-8201356 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 17 | rs562859917 | chr11:8201378-8201379 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 18 | rs7479156 | chr11:8201417-8201418 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 19 | rs565289849 | chr11:8201439-8201440 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 20 | rs527741224 | chr11:8201440-8201441 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:61)
| Disease | PMID | Source |
|---|---|---|
| Neuroblastoma | 18923191 | CNVD |
| Breast cancer | 19432969 | CNVD |
| Alzheimer''s disease | 17576883 | CNVD |
| Long-qt syndrome | 17576883 | CNVD |
| Emphysema | 19352772 | CNVD |
| Invasive pancreatic ductal carcinoma | 16982739 | CNVD |
| Chordoma | 18071362 | CNVD |
| Breast cancer | 16608533 | CNVD |
| Cancer | 21183584 | CNVD |
| Gastric adenocarcinoma | 19115996 | CNVD |
| Hepatocellular carcinoma | 16750200 | CNVD |
| Burkitt''s lymphoma | 19759907 | CNVD |
| Breast cancer | 17603634 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| Thyroid cancer | 19087340 | CNVD |
| Melanoma | 18172304 | CNVD |
| Basal cell lymphoma | 16317097 | CNVD |
| Diffuse large b-cell lymphoma | 16317097 | CNVD |
| Wilms tumour | 21544195 | CNVD |
| Parathyroid adenoma | 22454399 | CNVD |
| Chordoma | 21602918 | CNVD |
| Breast cancer | 21949216 | CNVD |
| Cancer | 21637783 | CNVD |
| Non-syndromic sensorineural hearing loss | 19222835 | CNVD |
| T-cell acute lymphoblastic leukemia | 20065082 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Astrocytoma | 17387387 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Beckwith-Wiedemann syndrome | 21518781 | CNVD |
| Wilms tumour | 21518781 | CNVD |
| Hepatoblastoma | 21518781 | CNVD |
| Acute lymphoblastic leukemia | 20067559 | CNVD |
| Gastrointestinal stromal cancer | 17535989 | CNVD |
| Paraganglioma | 17535989 | CNVD |
| Pulmonary chondroma | 17535989 | CNVD |
| Gastric cancer | 17908304 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Multiple myeloma | 20724749 | CNVD |
| Acute lymphoblastic leukemia | 20435627 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Autism | 22495311 | CNVD |
| Ovine squamous-cell carcinoma | 17599052 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Glioma | 17123091 | CNVD |
| Lung cancer | 16773561 | CNVD |
| Neuroblastoma | 21124317 | CNVD |
| Lung adenocarcinoma | 17086460 | CNVD |
| Lung cancer | 17086460 | CNVD |
| Schizophrenia | 21399695 | CNVD |
| Gastric cancer | 16891809 | CNVD |
| Cancer | 17160897 | CNVD |
| Multiple myeloma | 16616336 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Dysmorphic features | 22052655 | CNVD |
| Intellectual disability | 22052655 | CNVD |
| Obesity | 22052655 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| Pancreatic ductal adenocarcinoma | 19077451 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr11:8200200-8202000 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 2 | chr11:8200200-8202000 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
