| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58351501-58351737 | Common:1; Rare:57 | ||||
| chr17:58352134-58352425 | Common:5; Rare:122 | ||||
| chr17:58487595-58487921 | Common:2; Rare:85 | ||||
| chr17:58488321-58488517 | Rare:60 | ||||
| chr17:58508791-58508970 | Common:1; Rare:32 | ||||
| chr17:58513937-58514116 | Rare:31 | ||||
| chr17:58517831-58518219 | Common:1; Rare:93 | ||||
| chr17:58532036-58532113 | Rare:19 | ||||
| chr17:58540807-58540927 | Rare:17 | ||||
| chr17:58544292-58544428 | Rare:19 | ||||
| chr17:58692002-58692147 | Common:4; Rare:66 | ||||
| chr17:58692550-58692714 | Common:1; Rare:85; Clinvar:21; Clinvar (benign):21 | ||||
| chr17:58755632-58755994 | Rare:87 | ||||
| chr17:59106442-59106526 | Rare:29 | ||||
| chr17:59106530-59107033 | Common:3; Rare:155; Clinvar:7; Clinvar (benign):4 |