| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:54968595-54968799 | Common:3; Rare:95 | ||||
| chr17:56961005-56961329 | Common:4; Rare:74 | ||||
| chr17:56977981-56978157 | Common:3; Rare:85 | ||||
| chr17:57084976-57085383 | Rare:127 | ||||
| chr17:57256992-57257059 | Rare:26 | ||||
| chr17:57849968-57850282 | Common:1; Rare:109 | ||||
| chr17:57988122-57988536 | Common:5; Rare:121 | ||||
| chr17:58007118-58007384 | Common:1; Rare:124 | ||||
| chr17:58219216-58219401 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58328646-58328961 | Common:2; Rare:64 | ||||
| chr17:58352119-58352458 | Common:6; Rare:133 | ||||
| chr17:58531962-58532143 | Rare:43 | ||||
| chr17:58692528-58692685 | Common:1; Rare:84; Clinvar:16; Clinvar (benign):20 | ||||
| chr17:59106529-59107016 | Common:3; Rare:149; Clinvar:7; Clinvar (benign):4 | ||||
| chr17:59155143-59155450 | Common:2; Rare:76 |