| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:69414186-69414356 | Rare:45 | ||||
| chr15:69452691-69453020 | Common:5; Rare:137 | ||||
| chr15:70097890-70098104 | Common:1; Rare:49 | ||||
| chr15:70763437-70763725 | Common:2; Rare:99 | ||||
| chr15:70892492-70892885 | Common:1; Rare:94 | ||||
| chr15:71547215-71547365 | Rare:37 | ||||
| chr15:72118167-72118435 | Common:2; Rare:88 | ||||
| chr15:72231114-72231511 | Common:3; Rare:123 | ||||
| chr15:72375932-72376123 | Common:2; Rare:81; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:73752245-73752352 | Rare:30 | ||||
| chr15:73926304-73926466 | Rare:43 | ||||
| chr15:73994587-73994716 | Rare:20 | ||||
| chr15:74202724-74203023 | Rare:72; Clinvar:2 | ||||
| chr15:74461101-74461314 | Rare:66 | ||||
| chr15:74540966-74541271 | Common:4; Rare:108 |