| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:57849968-57850292 | Common:1; Rare:113 | ||||
| chr17:57988113-57988535 | Common:6; Rare:122 | ||||
| chr17:58007216-58007384 | Common:1; Rare:72 | ||||
| chr17:58219205-58219374 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58352083-58352486 | Common:6; Rare:146 | ||||
| chr17:58517838-58518217 | Common:1; Rare:90 | ||||
| chr17:58692549-58692709 | Common:1; Rare:84; Clinvar:21; Clinvar (benign):20 | ||||
| chr17:59106701-59107009 | Common:2; Rare:102; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59154982-59155291 | Common:1; Rare:100 | ||||
| chr17:59155425-59155784 | Rare:88 | ||||
| chr17:59331489-59331788 | Common:2; Rare:98 | ||||
| chr17:59619569-59620069 | Common:3; Rare:174 | ||||
| chr17:59683457-59683745 | Rare:42 | ||||
| chr17:59707381-59707742 | Common:4; Rare:100; Clinvar (benign):6 | ||||
| chr17:59837635-59838066 | Common:1; Rare:67 |