| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:55751307-55751426 | Common:2; Rare:41 | ||||
| chr17:56914015-56914180 | Rare:43 | ||||
| chr17:57084980-57085096 | Rare:40 | ||||
| chr17:57849995-57850281 | Common:1; Rare:94 | ||||
| chr17:57988138-57988491 | Common:5; Rare:109 | ||||
| chr17:58007199-58007386 | Common:1; Rare:82 | ||||
| chr17:58219198-58219372 | Common:1; Rare:69; Clinvar:3; Clinvar (benign):5 | ||||
| chr17:58692528-58692714 | Common:1; Rare:95; Clinvar:21; Clinvar (benign):21 | ||||
| chr17:59106685-59106999 | Common:2; Rare:107; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:59155129-59155427 | Common:2; Rare:79 | ||||
| chr17:59155536-59155781 | Rare:69 | ||||
| chr17:59619576-59619987 | Common:3; Rare:147 | ||||
| chr17:59619996-59620010 | Rare:3 | ||||
| chr17:59707397-59707727 | Common:3; Rare:90; Clinvar (benign):3 | ||||
| chr17:59837626-59837970 | Rare:48 |