| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1456058-1456560 | Common:8; Rare:194 | ||||
| chr17:1463256-1463561 | Common:2; Rare:74 | ||||
| chr17:1470432-1470514 | Common:1; Rare:28; Clinvar (benign):1 | ||||
| chr17:1485718-1486196 | Common:4; Rare:150 | ||||
| chr17:1486884-1487095 | Rare:48 | ||||
| chr17:1487202-1487335 | Common:1; Rare:38 | ||||
| chr17:1490700-1491148 | Common:5; Rare:94 | ||||
| chr17:1491174-1491339 | Common:1; Rare:44 | ||||
| chr17:1491666-1491779 | Common:1; Rare:33 | ||||
| chr17:1515738-1516072 | Common:1; Rare:67 | ||||
| chr17:1516553-1516965 | Common:3; Rare:147 | ||||
| chr17:1562651-1562996 | Common:3; Rare:105 | ||||
| chr17:1628410-1628553 | Rare:47 | ||||
| chr17:1628801-1629026 | Rare:79 | ||||
| chr17:1648894-1649244 | Common:3; Rare:120 |