| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72783447-72783816 | Common:2; Rare:139 | ||||
| chr15:73633189-73633321 | Rare:59 | ||||
| chr15:73633348-73633475 | Common:1; Rare:41 | ||||
| chr15:73994556-73994802 | Common:1; Rare:51 | ||||
| chr15:74461101-74461314 | Rare:66 | ||||
| chr15:74540966-74541283 | Common:4; Rare:112 | ||||
| chr15:74598355-74598511 | Common:1; Rare:64 | ||||
| chr15:74615559-74615898 | Common:4; Rare:107 | ||||
| chr15:74695973-74696077 | Rare:34 | ||||
| chr15:74843110-74843233 | Common:1; Rare:35 | ||||
| chr15:74873299-74873553 | Common:6; Rare:70 | ||||
| chr15:74889920-74890076 | Rare:57; Clinvar (pathogenic):1 | ||||
| chr15:74906735-74906881 | Common:1; Rare:60 | ||||
| chr15:74937987-74938254 | Common:2; Rare:91 | ||||
| chr15:74995434-74995615 | Common:4; Rare:78 |