| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59685361-59685680 | Common:2; Rare:67 | ||||
| chr17:59707378-59707747 | Common:4; Rare:104; Clinvar (benign):6 | ||||
| chr17:59837635-59838385 | Common:4; Rare:134 | ||||
| chr17:59892709-59893179 | Common:1; Rare:130 | ||||
| chr17:59964690-59965096 | Common:2; Rare:126 | ||||
| chr17:60078910-60079005 | Common:4; Rare:44 | ||||
| chr17:60391946-60392279 | Common:2; Rare:94 | ||||
| chr17:60525918-60526339 | Common:2; Rare:148 | ||||
| chr17:60886909-60887120 | Common:4; Rare:61 | ||||
| chr17:61157363-61157463 | Rare:18 | ||||
| chr17:61400333-61400405 | Rare:34 | ||||
| chr17:61863433-61863666 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:62423782-62423981 | Common:1; Rare:77 | ||||
| chr17:63550137-63550671 | Common:3; Rare:120 | ||||
| chr17:63600811-63600937 | Rare:34; Clinvar:2 |