| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58352125-58352473 | Common:6; Rare:135 | ||||
| chr17:58517823-58518060 | Common:1; Rare:55 | ||||
| chr17:58691996-58692161 | Common:4; Rare:74 | ||||
| chr17:58692486-58692761 | Common:3; Rare:143; Clinvar:29; Clinvar (benign):28; Clinvar (pathogenic):2 | ||||
| chr17:58755762-58755984 | Rare:65 | ||||
| chr17:59106639-59107153 | Common:3; Rare:161; Clinvar:6; Clinvar (benign):4 | ||||
| chr17:59154952-59155025 | Rare:31 | ||||
| chr17:59155101-59155841 | Common:2; Rare:183 | ||||
| chr17:59220364-59220607 | Common:4; Rare:68 | ||||
| chr17:59565469-59565746 | Common:1; Rare:102 | ||||
| chr17:59619254-59619333 | Rare:20 | ||||
| chr17:59619532-59620134 | Common:3; Rare:213 | ||||
| chr17:59707378-59707736 | Common:4; Rare:101; Clinvar (benign):6 | ||||
| chr17:59892715-59893248 | Common:1; Rare:152 | ||||
| chr17:59964706-59965092 | Common:2; Rare:118 |