| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:69414060-69414444 | Common:1; Rare:112 | ||||
| chr15:70763436-70763840 | Common:2; Rare:134 | ||||
| chr15:70854101-70854293 | Rare:64 | ||||
| chr15:70892381-70892721 | Common:1; Rare:75 | ||||
| chr15:72118184-72118432 | Common:2; Rare:78 | ||||
| chr15:72231123-72231523 | Common:3; Rare:129 | ||||
| chr15:72375968-72376118 | Common:1; Rare:64; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr15:72686091-72686220 | Common:2; Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73633225-73633305 | Rare:33 | ||||
| chr15:73633354-73633595 | Common:2; Rare:81 | ||||
| chr15:73994600-73994813 | Rare:44 | ||||
| chr15:74461101-74461314 | Rare:66 | ||||
| chr15:74540966-74541247 | Common:3; Rare:96 | ||||
| chr15:74615597-74615898 | Common:4; Rare:98 | ||||
| chr15:74695948-74696138 | Rare:60 |