| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:13031807-13032207 | Common:5; Rare:101 | ||||
| chr17:13347491-13347693 | Common:2; Rare:43 | ||||
| chr17:14302580-14302840 | Common:1; Rare:77 | ||||
| chr17:15171560-15171800 | Common:1; Rare:49 | ||||
| chr17:15257498-15257602 | Common:2; Rare:25 | ||||
| chr17:15377740-15378120 | Rare:63 | ||||
| chr17:15490730-15490878 | Common:1; Rare:30 | ||||
| chr17:15920990-15921460 | Common:4; Rare:84 | ||||
| chr17:15945872-15946272 | Common:2; Rare:115 | ||||
| chr17:15957302-15957505 | Common:1; Rare:39 | ||||
| chr17:15959225-15959529 | Rare:38 | ||||
| chr17:15963729-15963915 | Rare:30 | ||||
| chr17:15963930-15964125 | Common:1; Rare:40 | ||||
| chr17:15966315-15966464 | Rare:27 | ||||
| chr17:16028129-16028529 | Common:4; Rare:136; Clinvar:5; Clinvar (benign):4 |