| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:55722732-55722991 | Common:2; Rare:53 | ||||
| chr17:56833784-56834128 | Common:4; Rare:91 | ||||
| chr17:56914005-56914180 | Common:1; Rare:45 | ||||
| chr17:56978031-56978207 | Common:3; Rare:85 | ||||
| chr17:57084959-57085346 | Common:1; Rare:127 | ||||
| chr17:57255703-57255879 | Common:2; Rare:40 | ||||
| chr17:57849965-57850274 | Common:1; Rare:108 | ||||
| chr17:57988155-57988512 | Common:5; Rare:107 | ||||
| chr17:58007199-58007557 | Common:1; Rare:132 | ||||
| chr17:58007632-58007836 | Rare:52 | ||||
| chr17:58219212-58219372 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58351446-58351749 | Common:1; Rare:71 | ||||
| chr17:58352119-58352409 | Common:5; Rare:124 | ||||
| chr17:58692559-58692668 | Common:1; Rare:62; Clinvar:10; Clinvar (benign):20 | ||||
| chr17:59106699-59106999 | Common:2; Rare:102; Clinvar:4; Clinvar (benign):2 |