| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:31314081-31314337 | Rare:42 | ||||
| chr17:31318370-31318761 | Rare:130; Clinvar (benign):1 | ||||
| chr17:31487707-31488156 | Rare:139 | ||||
| chr17:31488210-31488319 | Rare:32 | ||||
| chr17:31488679-31488720 | Rare:8 | ||||
| chr17:31858163-31858469 | Common:1; Rare:59 | ||||
| chr17:31858734-31859004 | Common:3; Rare:68 | ||||
| chr17:31859153-31859388 | Common:3; Rare:69 | ||||
| chr17:31900917-31901049 | Rare:25 | ||||
| chr17:31901587-31901987 | Common:3; Rare:118 | ||||
| chr17:31936747-31937227 | Common:1; Rare:144 | ||||
| chr17:32007201-32007446 | Rare:75 | ||||
| chr17:32007548-32007668 | Common:2; Rare:27 | ||||
| chr17:32007773-32007954 | Common:1; Rare:49 | ||||
| chr17:32142041-32142201 | Common:1; Rare:36 |