| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75426340-75426670 | Rare:72 | ||||
| chr17:75472171-75472480 | Common:2; Rare:55 | ||||
| chr17:75514215-75514531 | Common:1; Rare:81 | ||||
| chr17:75517486-75518018 | Common:10; Rare:215; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:75526556-75527137 | Common:9; Rare:164 | ||||
| chr17:75549313-75549762 | Common:13; Rare:221 | ||||
| chr17:75549820-75550224 | Common:14; Rare:162 | ||||
| chr17:75589108-75589594 | Common:45; Rare:353 | ||||
| chr17:75642720-75643260 | Rare:82 | ||||
| chr17:75780740-75781497 | Rare:255 | ||||
| chr17:75783143-75783755 | Common:7; Rare:157 | ||||
| chr17:75808977-75809325 | Common:4; Rare:73 | ||||
| chr17:75872820-75873080 | Common:1; Rare:93 | ||||
| chr17:76025430-76025770 | Common:3; Rare:74 | ||||
| chr17:76097848-76098251 | Common:2; Rare:215 |