| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:57084980-57085119 | Rare:47 | ||||
| chr17:57850002-57850274 | Common:1; Rare:89 | ||||
| chr17:58352134-58352234 | Common:1; Rare:51 | ||||
| chr17:58692550-58692650 | Common:1; Rare:54; Clinvar:5; Clinvar (benign):16 | ||||
| chr17:59106701-59107015 | Common:2; Rare:105; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59155100-59155781 | Common:2; Rare:175 | ||||
| chr17:59565469-59565683 | Common:1; Rare:84 | ||||
| chr17:59619181-59619373 | Common:2; Rare:54 | ||||
| chr17:59619562-59620107 | Common:3; Rare:188 | ||||
| chr17:59707397-59707732 | Common:3; Rare:91; Clinvar (benign):3 | ||||
| chr17:59837626-59838051 | Rare:62 | ||||
| chr17:59838228-59838392 | Rare:41 | ||||
| chr17:59892882-59893140 | Rare:75 | ||||
| chr17:59964712-59964826 | Common:2; Rare:47 | ||||
| chr17:60078910-60079005 | Common:4; Rare:44 |