| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68512210-68512541 | Common:2; Rare:108; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:69327091-69327334 | Common:2; Rare:81 | ||||
| chr17:70169344-70169539 | Common:1; Rare:52 | ||||
| chr17:73192817-73193067 | Common:15; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232109-73232726 | Common:4; Rare:237 | ||||
| chr17:74776281-74776550 | Common:4; Rare:89 | ||||
| chr17:75012565-75012755 | Common:2; Rare:59 | ||||
| chr17:75046929-75047171 | Common:1; Rare:74 | ||||
| chr17:75109853-75109982 | Common:2; Rare:36 | ||||
| chr17:75205370-75205767 | Common:1; Rare:132 | ||||
| chr17:75261580-75261951 | Common:4; Rare:120; Clinvar (benign):3 | ||||
| chr17:75271157-75271390 | Common:3; Rare:41 | ||||
| chr17:75289377-75289606 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:75393746-75394020 | Common:1; Rare:66 | ||||
| chr17:75456465-75456656 | Rare:51 |