Variant report
| Variant | rs73598786 |
|---|---|
| Chromosome Location | chr16:82023884-82023885 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr16:82021600-82029600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 2 | chr16:82021800-82030000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 3 | chr16:82022000-82030000 | Weak transcription | Duodenum Mucosa | Duodenum |
| 4 | chr16:82023000-82027800 | Weak transcription | Primary T cells from cord blood | blood |
| 5 | chr16:82023000-82031800 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
| 6 | chr16:82023600-82025200 | Enhancers | Fetal Intestine Large | intestine |
| 7 | chr16:82023600-82036600 | Weak transcription | Fetal Kidney | kidney |
| 8 | chr16:82023800-82026200 | Enhancers | Fetal Intestine Small | intestine |
| 9 | chr16:82023800-82027800 | Weak transcription | Pancreas | Pancrea |
