| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72231285-72231516 | Common:3; Rare:60 | ||||
| chr15:72246025-72246283 | Rare:54 | ||||
| chr15:72375929-72376128 | Common:2; Rare:81; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72474757-72475004 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr15:73563233-73563445 | Common:1; Rare:50 | ||||
| chr15:73632477-73632523 | Rare:10 | ||||
| chr15:73633166-73633622 | Common:2; Rare:178 | ||||
| chr15:73711107-73711169 | Rare:26 | ||||
| chr15:73926302-73926503 | Rare:54 | ||||
| chr15:73994578-73994819 | Common:1; Rare:51 | ||||
| chr15:74461086-74461347 | Rare:77 | ||||
| chr15:74540918-74541283 | Common:4; Rare:127 | ||||
| chr15:74615559-74615901 | Common:4; Rare:108 | ||||
| chr15:74695923-74696144 | Rare:68 | ||||
| chr15:74725453-74725596 | Rare:16 |