| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:79310766-79311297 | Common:5; Rare:157 | ||||
| chr15:79431885-79432118 | Common:2; Rare:57 | ||||
| chr15:79896642-79897127 | Common:10; Rare:195; Clinvar (pathogenic):1 | ||||
| chr15:79897160-79897410 | Common:3; Rare:51 | ||||
| chr15:79923117-79923273 | Common:4; Rare:71 | ||||
| chr15:79923510-79924115 | Common:9; Rare:225 | ||||
| chr15:79924118-79924214 | Common:3; Rare:19 | ||||
| chr15:80059401-80059776 | Common:1; Rare:125 | ||||
| chr15:80059858-80060144 | Common:1; Rare:104 | ||||
| chr15:80060245-80060287 | Rare:16 | ||||
| chr15:80404185-80404405 | Rare:63 | ||||
| chr15:80695038-80695202 | Rare:56 | ||||
| chr15:80695690-80695812 | Rare:31 | ||||
| chr15:80779253-80779372 | Common:1; Rare:24 | ||||
| chr15:80989553-80989611 | Common:1; Rare:21 |