| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59839142-59839315 | Rare:42 | ||||
| chr17:59884068-59884257 | Common:1; Rare:44 | ||||
| chr17:59893674-59893921 | Rare:36 | ||||
| chr17:60134868-60135084 | Rare:33 | ||||
| chr17:60227524-60227569 | Rare:7 | ||||
| chr17:60228470-60228482 | Rare:1 | ||||
| chr17:60245343-60245421 | Common:1; Rare:13 | ||||
| chr17:60255217-60255289 | Rare:23 | ||||
| chr17:60477827-60477907 | Rare:15 | ||||
| chr17:60518953-60519130 | Common:3; Rare:48 | ||||
| chr17:60522255-60522283 | Rare:5 | ||||
| chr17:60522893-60522913 | Rare:3 | ||||
| chr17:60601294-60601588 | Common:2; Rare:62 | ||||
| chr17:60601951-60602188 | Rare:34; Clinvar (benign):1 | ||||
| chr17:60615552-60615661 | Rare:17 |