| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28719490-28720132 | Common:6; Rare:819 | ||||
| chr17:28720427-28720881 | Common:2; Rare:416 | ||||
| chr17:28722723-28723506 | Common:8; Rare:297 | ||||
| chr17:28723428-28723733 | Common:2; Rare:110 | ||||
| chr17:28723732-28724132 | Common:2; Rare:122 | ||||
| chr17:28725189-28725589 | Common:1; Rare:163 | ||||
| chr17:28725575-28726503 | Common:33; Rare:906 | ||||
| chr17:28726470-28726670 | Common:2; Rare:59 | ||||
| chr17:28726780-28727404 | Common:14; Rare:592 | ||||
| chr17:28727925-28728249 | Rare:83 | ||||
| chr17:28728177-28728277 | Rare:21 | ||||
| chr17:28728603-28728870 | Rare:449; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:28728867-28729220 | Common:10; Rare:314 | ||||
| chr17:28735273-28735673 | Common:3; Rare:162; Clinvar:4 | ||||
| chr17:28743437-28743551 | Rare:15 |