Variant report
| Variant | rs59765747 |
|---|---|
| Chromosome Location | chr9:100469821-100469822 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:100462400-100472800 | Weak transcription | Brain Substantia Nigra | brain |
| 2 | chr9:100466800-100472800 | Weak transcription | K562 | blood |
| 3 | chr9:100467200-100472800 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
| 4 | chr9:100467200-100476400 | Weak transcription | Fetal Intestine Large | intestine |
| 5 | chr9:100468000-100472600 | Weak transcription | Hela-S3 | cervix |
| 6 | chr9:100468000-100476600 | Weak transcription | GM12878-XiMat | blood |
| 7 | chr9:100468600-100472800 | Weak transcription | Primary T cells effector/memory enriched fromperipheralblood | blood |
| 8 | chr9:100468600-100473200 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
| 9 | chr9:100468800-100472800 | Weak transcription | Primary T helper memory cells from peripheral blood 1 | blood |
| 10 | chr9:100469600-100473000 | Weak transcription | Primary T helper naive cells from peripheral blood | blood |
