| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72231396-72231447 | Common:1; Rare:15 | ||||
| chr15:72375951-72376118 | Common:2; Rare:74; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr15:73926322-73926482 | Rare:45 | ||||
| chr15:73994587-73994795 | Rare:45 | ||||
| chr15:74202747-74203018 | Rare:69; Clinvar:2 | ||||
| chr15:74461103-74461323 | Rare:66 | ||||
| chr15:74540966-74541276 | Common:4; Rare:109 | ||||
| chr15:74598305-74598520 | Common:1; Rare:90 | ||||
| chr15:74695973-74696093 | Rare:40 | ||||
| chr15:74889958-74890067 | Rare:43 | ||||
| chr15:75451671-75452010 | Common:1; Rare:91 | ||||
| chr15:75625612-75625906 | Common:2; Rare:70 | ||||
| chr15:75640212-75640507 | Common:2; Rare:78 | ||||
| chr15:75647865-75648023 | Common:1; Rare:38 | ||||
| chr15:75649673-75649936 | Common:1; Rare:56 |