| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50152487-50152814 | Common:1; Rare:62 | ||||
| chr17:50154838-50154913 | Rare:10 | ||||
| chr17:50161471-50161793 | Common:2; Rare:88 | ||||
| chr17:50193017-50193227 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:50421458-50421592 | Common:1; Rare:16 | ||||
| chr17:50426997-50427124 | Rare:12 | ||||
| chr17:50427500-50427663 | Rare:28 | ||||
| chr17:50542038-50542299 | Rare:101 | ||||
| chr17:50632735-50632825 | Rare:17 | ||||
| chr17:50708881-50708959 | Common:1; Rare:7 | ||||
| chr17:50763220-50763407 | Common:1; Rare:32 | ||||
| chr17:50828557-50828710 | Rare:31 | ||||
| chr17:50865530-50865760 | Rare:46 | ||||
| chr17:50867226-50867360 | Rare:25 | ||||
| chr17:51119987-51120158 | Common:1; Rare:37 |