| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:56913371-56913515 | Common:1; Rare:44 | ||||
| chr17:56913984-56914186 | Common:1; Rare:58 | ||||
| chr17:56978031-56978187 | Common:3; Rare:82 | ||||
| chr17:57084959-57085392 | Common:2; Rare:135 | ||||
| chr17:57256902-57257048 | Rare:48 | ||||
| chr17:57257227-57257546 | Common:6; Rare:59 | ||||
| chr17:57849968-57850292 | Common:1; Rare:113 | ||||
| chr17:57988164-57988524 | Common:5; Rare:106 | ||||
| chr17:58006472-58006675 | Common:1; Rare:67 | ||||
| chr17:58006946-58007384 | Common:1; Rare:147 | ||||
| chr17:58083212-58083604 | Common:4; Rare:150 | ||||
| chr17:58219207-58219374 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58352131-58352495 | Common:6; Rare:138 | ||||
| chr17:58531976-58532169 | Common:1; Rare:47 | ||||
| chr17:58692549-58692668 | Common:1; Rare:67; Clinvar:10; Clinvar (benign):20 |