Variant report
| Variant | rs73695662 |
|---|---|
| Chromosome Location | chr7:50490656-50490657 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:50485000-50490800 | Weak transcription | Spleen | Spleen |
| 2 | chr7:50486200-50513200 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
| 3 | chr7:50486400-50491600 | Weak transcription | Primary B cells from peripheral blood | blood |
| 4 | chr7:50486600-50495000 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
| 5 | chr7:50486800-50491400 | Weak transcription | Fetal Thymus | thymus |
| 6 | chr7:50489400-50491000 | Enhancers | HUVEC | blood vessel |
| 7 | chr7:50490400-50491200 | Enhancers | Primary mononuclear cells fromperipheralblood | Blood |
