| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1279394-1279731 | Common:1; Rare:87 | ||||
| chr17:1279856-1280002 | Common:1; Rare:49 | ||||
| chr17:1398939-1399197 | Common:1; Rare:84 | ||||
| chr17:1400057-1400356 | Common:3; Rare:123 | ||||
| chr17:1455920-1455986 | Rare:15 | ||||
| chr17:1456152-1456498 | Common:6; Rare:137 | ||||
| chr17:1467987-1468325 | Common:3; Rare:124; Clinvar (benign):5 | ||||
| chr17:1470483-1470813 | Common:2; Rare:132 | ||||
| chr17:1478162-1478249 | Common:1; Rare:31 | ||||
| chr17:1480580-1480887 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr17:1485720-1486002 | Common:3; Rare:103 | ||||
| chr17:1491200-1491306 | Common:1; Rare:23 | ||||
| chr17:1491601-1491816 | Common:1; Rare:63 | ||||
| chr17:1492012-1492064 | Rare:14 | ||||
| chr17:1492568-1492772 | Common:1; Rare:38 |