| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50707976-50708013 | Rare:6 | ||||
| chr17:50719417-50719661 | Common:1; Rare:98 | ||||
| chr17:51166245-51166577 | Common:3; Rare:82 | ||||
| chr17:51260148-51260598 | Common:3; Rare:167 | ||||
| chr17:54968601-54968799 | Common:3; Rare:92 | ||||
| chr17:55751335-55751426 | Common:1; Rare:33 | ||||
| chr17:56914022-56914191 | Rare:44 | ||||
| chr17:56978024-56978168 | Common:3; Rare:72 | ||||
| chr17:57084956-57085090 | Common:1; Rare:45 | ||||
| chr17:57850002-57850274 | Common:1; Rare:89 | ||||
| chr17:58007205-58007384 | Common:1; Rare:77 | ||||
| chr17:58219223-58219341 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:58352131-58352343 | Common:4; Rare:98 | ||||
| chr17:58517838-58517950 | Common:1; Rare:24 | ||||
| chr17:58692528-58692702 | Common:1; Rare:89; Clinvar:19; Clinvar (benign):20 |