| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:29145454-29145586 | Common:1; Rare:20 | ||||
| chr17:29148727-29149206 | Common:2; Rare:121 | ||||
| chr17:29149580-29149782 | Rare:28 | ||||
| chr17:29292315-29292496 | Common:2; Rare:32 | ||||
| chr17:29292700-29293108 | Common:3; Rare:145 | ||||
| chr17:29590499-29590560 | Rare:13 | ||||
| chr17:29706478-29706605 | Rare:19 | ||||
| chr17:29706797-29707143 | Rare:82 | ||||
| chr17:29760365-29760590 | Common:2; Rare:38 | ||||
| chr17:30212727-30212992 | Rare:66; Clinvar (benign):1 | ||||
| chr17:30213396-30213545 | Rare:27 | ||||
| chr17:30332241-30332394 | Common:1; Rare:30 | ||||
| chr17:30363843-30364124 | Common:2; Rare:43 | ||||
| chr17:30551015-30551214 | Common:1; Rare:43 | ||||
| chr17:30600058-30600205 | Common:1; Rare:25 |