| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:409928-410498 | Common:10; Rare:253 | ||||
| chr17:410695-410727 | Rare:10 | ||||
| chr17:714195-714316 | Rare:24 | ||||
| chr17:714563-715046 | Common:5; Rare:156; Clinvar (benign):3 | ||||
| chr17:715165-715179 | Common:1 | ||||
| chr17:715305-715391 | Rare:15 | ||||
| chr17:731864-731937 | Rare:16 | ||||
| chr17:732077-732728 | Common:2; Rare:222 | ||||
| chr17:732926-733287 | Common:5; Rare:140 | ||||
| chr17:733319-733387 | Rare:11 | ||||
| chr17:751446-751850 | Rare:93 | ||||
| chr17:751882-752043 | Common:1; Rare:45 | ||||
| chr17:752132-752444 | Common:3; Rare:129 | ||||
| chr17:781656-781908 | Common:1; Rare:53 | ||||
| chr17:781955-782598 | Common:5; Rare:277 |