| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68512302-68512548 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:68955244-68955471 | Rare:41 | ||||
| chr17:69060972-69061289 | Common:2; Rare:44 | ||||
| chr17:69327072-69327338 | Common:2; Rare:89 | ||||
| chr17:70169327-70169554 | Common:1; Rare:61 | ||||
| chr17:72120784-72121034 | Rare:67 | ||||
| chr17:73164831-73165084 | Common:2; Rare:70 | ||||
| chr17:73192823-73193070 | Common:14; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232100-73232707 | Common:4; Rare:230 | ||||
| chr17:73311949-73312232 | Rare:74 | ||||
| chr17:74213253-74213583 | Common:4; Rare:71 | ||||
| chr17:74466578-74466685 | Rare:31 | ||||
| chr17:74748438-74748651 | Common:2; Rare:76 | ||||
| chr17:74776265-74776543 | Common:4; Rare:93 | ||||
| chr17:75032433-75032620 | Common:1; Rare:23 |