| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:54962761-54963060 | Common:1; Rare:66 | ||||
| chr17:54968292-54968799 | Common:3; Rare:203 | ||||
| chr17:56833847-56834151 | Common:3; Rare:86 | ||||
| chr17:56913441-56913591 | Rare:44 | ||||
| chr17:56913995-56914176 | Common:1; Rare:49 | ||||
| chr17:57084985-57085368 | Rare:122 | ||||
| chr17:57256628-57256775 | Rare:20 | ||||
| chr17:57257008-57257038 | Rare:12 | ||||
| chr17:57849980-57850282 | Common:1; Rare:101 | ||||
| chr17:57955241-57955323 | Rare:19 | ||||
| chr17:57955661-57955977 | Common:2; Rare:52 | ||||
| chr17:58006329-58006685 | Common:2; Rare:95 | ||||
| chr17:58007008-58007560 | Common:1; Rare:190 | ||||
| chr17:58352089-58352257 | Common:1; Rare:67 | ||||
| chr17:58692558-58692715 | Common:1; Rare:83; Clinvar:22; Clinvar (benign):21 |