| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:67717745-67717977 | Rare:82 | ||||
| chr17:67826246-67826258 | Rare:3 | ||||
| chr17:68247928-68248137 | Common:5; Rare:89 | ||||
| chr17:68248433-68248643 | Common:1; Rare:39 | ||||
| chr17:68291262-68291509 | Common:1; Rare:69 | ||||
| chr17:68511614-68512137 | Common:5; Rare:136 | ||||
| chr17:68512273-68512548 | Common:1; Rare:97; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:68512681-68512951 | Rare:97 | ||||
| chr17:68515136-68515573 | Common:3; Rare:117; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):5 | ||||
| chr17:68955223-68955527 | Rare:52 | ||||
| chr17:69141803-69142040 | Common:2; Rare:50 | ||||
| chr17:69327066-69327338 | Common:2; Rare:90 | ||||
| chr17:69414627-69414752 | Rare:26 | ||||
| chr17:70169300-70169557 | Common:1; Rare:74 | ||||
| chr17:72120783-72121047 | Rare:70 |