| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28727387-28727506 | Rare:22 | ||||
| chr17:28727953-28728002 | Rare:8 | ||||
| chr17:28728065-28728366 | Common:1; Rare:68 | ||||
| chr17:28728583-28728844 | Rare:81; Clinvar (benign):1 | ||||
| chr17:28728850-28729176 | Common:2; Rare:81; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:28743119-28743703 | Rare:98 | ||||
| chr17:28743800-28744110 | Common:4; Rare:93 | ||||
| chr17:28744365-28744536 | Common:1; Rare:42 | ||||
| chr17:28744626-28744668 | Rare:7 | ||||
| chr17:28811794-28811854 | Common:1; Rare:14 | ||||
| chr17:28812248-28812823 | Common:3; Rare:149 | ||||
| chr17:28812854-28813102 | Common:3; Rare:35 | ||||
| chr17:28842380-28842393 | Rare:1 | ||||
| chr17:28842507-28842921 | Common:3; Rare:122 | ||||
| chr17:28854844-28855101 | Rare:70 |