| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:51260855-51260978 | Common:2; Rare:55 | ||||
| chr17:54968571-54968799 | Common:3; Rare:103 | ||||
| chr17:56913390-56913554 | Common:1; Rare:48 | ||||
| chr17:56913989-56914186 | Common:1; Rare:57 | ||||
| chr17:57084980-57085339 | Rare:120 | ||||
| chr17:57849977-57850270 | Common:1; Rare:99 | ||||
| chr17:58007178-58007382 | Common:1; Rare:94 | ||||
| chr17:58219201-58219387 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):5 | ||||
| chr17:58347562-58347833 | Rare:52 | ||||
| chr17:58352093-58352352 | Common:4; Rare:112 | ||||
| chr17:58692541-58692668 | Common:1; Rare:70; Clinvar:10; Clinvar (benign):20 | ||||
| chr17:59106659-59106970 | Common:3; Rare:100; Clinvar:6; Clinvar (benign):4 | ||||
| chr17:59155159-59155334 | Common:1; Rare:45 | ||||
| chr17:59155447-59155758 | Rare:76 | ||||
| chr17:59331486-59331756 | Common:2; Rare:88 |