| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58326859-58327071 | Common:1; Rare:49 | ||||
| chr19:58327227-58327356 | Rare:28 | ||||
| chr19:58347591-58347782 | Common:8; Rare:91 | ||||
| chr19:58362735-58362781 | Common:1; Rare:23 | ||||
| chr19:58362807-58362970 | Common:1; Rare:47 | ||||
| chr19:58381003-58381367 | Common:6; Rare:82 | ||||
| chr19:58386719-58386820 | Common:2; Rare:32 | ||||
| chr19:58408449-58408763 | Common:4; Rare:95 | ||||
| chr19:58440134-58440482 | Common:6; Rare:93 | ||||
| chr19:58451458-58451660 | Common:2; Rare:78 | ||||
| chr19:58466871-58467115 | Common:1; Rare:78 | ||||
| chr19:58476004-58476180 | Common:1; Rare:68 | ||||
| chr19:58499211-58499644 | Common:2; Rare:154; Clinvar:6; Clinvar (benign):1 | ||||
| chr19:58519767-58520017 | Rare:65 | ||||
| chr19:58554195-58554376 | Rare:52 |