| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:81928017-81928176 | Common:1; Rare:26 | ||||
| chr17:81936536-81936576 | Rare:7 | ||||
| chr17:81936682-81936791 | Common:1; Rare:34; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:81937055-81937558 | Rare:165 | ||||
| chr17:81937592-81937698 | Rare:19 | ||||
| chr17:81959516-81959562 | Rare:12 | ||||
| chr17:81959745-81959892 | Common:2; Rare:42 | ||||
| chr17:81961171-81961495 | Common:2; Rare:117 | ||||
| chr17:81976548-81976839 | Common:3; Rare:67 | ||||
| chr17:81977393-81977803 | Common:1; Rare:151 | ||||
| chr17:81978078-81978133 | Common:1; Rare:19 | ||||
| chr17:82022687-82023343 | Common:9; Rare:238 | ||||
| chr17:82031043-82031232 | Common:1; Rare:63 | ||||
| chr17:82031528-82031744 | Common:1; Rare:88 | ||||
| chr17:82031764-82031809 | Rare:6 |