| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:56833930-56834187 | Common:2; Rare:92 | ||||
| chr17:56914029-56914177 | Rare:36 | ||||
| chr17:56977978-56978168 | Common:4; Rare:90 | ||||
| chr17:57084959-57085390 | Common:2; Rare:134 | ||||
| chr17:57256977-57257065 | Rare:33 | ||||
| chr17:57849965-57850285 | Common:1; Rare:112 | ||||
| chr17:57988155-57988536 | Common:5; Rare:111 | ||||
| chr17:58007205-58007390 | Common:1; Rare:79 | ||||
| chr17:58219216-58219374 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58352132-58352440 | Common:5; Rare:128 | ||||
| chr17:58531972-58532165 | Common:1; Rare:49 | ||||
| chr17:58692549-58692685 | Common:1; Rare:75; Clinvar:16; Clinvar (benign):20 | ||||
| chr17:59106701-59107001 | Common:2; Rare:101; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59155124-59155784 | Common:2; Rare:170 | ||||
| chr17:59331571-59331796 | Common:1; Rare:80 |