| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:56833894-56834231 | Common:3; Rare:112 | ||||
| chr17:56914029-56914168 | Rare:33 | ||||
| chr17:57084992-57085335 | Rare:118 | ||||
| chr17:57849991-57850274 | Common:1; Rare:94 | ||||
| chr17:58219216-58219304 | Common:1; Rare:35; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58352125-58352347 | Common:4; Rare:103 | ||||
| chr17:58531976-58532216 | Common:1; Rare:67 | ||||
| chr17:59106707-59106999 | Common:2; Rare:98; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59155143-59155517 | Common:2; Rare:83 | ||||
| chr17:59331452-59331803 | Common:2; Rare:115 | ||||
| chr17:59619563-59620057 | Common:3; Rare:173 | ||||
| chr17:59647980-59648271 | Common:1; Rare:50 | ||||
| chr17:59707386-59707727 | Common:3; Rare:95; Clinvar (benign):4 | ||||
| chr17:59837506-59838032 | Common:1; Rare:76 | ||||
| chr17:59892877-59893254 | Common:1; Rare:116 |