| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75271083-75271354 | Common:3; Rare:53 | ||||
| chr17:75393694-75394064 | Common:1; Rare:91 | ||||
| chr17:75456465-75456666 | Rare:55 | ||||
| chr17:75515459-75515639 | Common:3; Rare:52 | ||||
| chr17:75525509-75525717 | Common:2; Rare:64 | ||||
| chr17:75667100-75667507 | Common:5; Rare:135 | ||||
| chr17:75758332-75758534 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:75779042-75779405 | Common:2; Rare:155 | ||||
| chr17:75904854-75905204 | Common:4; Rare:99 | ||||
| chr17:75979096-75979315 | Rare:60; Clinvar:4 | ||||
| chr17:75979381-75979619 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr17:76060387-76060592 | Rare:57 | ||||
| chr17:76072317-76072533 | Common:6; Rare:130 | ||||
| chr17:76084005-76084286 | Rare:63 | ||||
| chr17:76103694-76103887 | Common:6; Rare:66 |