| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58007218-58007390 | Common:1; Rare:73 | ||||
| chr17:58219223-58219376 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:58352125-58352234 | Common:1; Rare:55 | ||||
| chr17:58692530-58692651 | Common:1; Rare:64; Clinvar:5; Clinvar (benign):17 | ||||
| chr17:59106701-59106999 | Common:2; Rare:101; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59155129-59155549 | Common:2; Rare:100 | ||||
| chr17:59331481-59331756 | Common:2; Rare:90 | ||||
| chr17:59619538-59620058 | Common:3; Rare:186 | ||||
| chr17:59707402-59707732 | Common:3; Rare:89; Clinvar (benign):2 | ||||
| chr17:59837609-59838032 | Rare:60 | ||||
| chr17:59892891-59893161 | Common:1; Rare:80 | ||||
| chr17:59964699-59965044 | Common:2; Rare:104 | ||||
| chr17:60078906-60078974 | Common:4; Rare:36 | ||||
| chr17:60525930-60526290 | Common:2; Rare:120 | ||||
| chr17:61452257-61452433 | Rare:47 |