| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59106659-59107126 | Common:3; Rare:151; Clinvar:6; Clinvar (benign):4 | ||||
| chr17:59154955-59155025 | Rare:30 | ||||
| chr17:59155102-59155340 | Common:1; Rare:68 | ||||
| chr17:59155404-59155792 | Rare:97 | ||||
| chr17:59619583-59620058 | Common:3; Rare:170 | ||||
| chr17:59707397-59707732 | Common:3; Rare:91; Clinvar (benign):3 | ||||
| chr17:59837634-59837994 | Rare:54 | ||||
| chr17:59892715-59893146 | Rare:117 | ||||
| chr17:59964706-59965111 | Common:2; Rare:120 | ||||
| chr17:60078910-60078984 | Common:4; Rare:39 | ||||
| chr17:60525930-60526290 | Common:2; Rare:120 | ||||
| chr17:62628028-62628166 | Rare:23 | ||||
| chr17:63550178-63550513 | Common:2; Rare:74 | ||||
| chr17:63600773-63600922 | Rare:40; Clinvar:2 | ||||
| chr17:63773478-63773842 | Common:2; Rare:119 |