| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88856901-88857199 | Common:4; Rare:152; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:88857551-88857628 | Common:1; Rare:27 | ||||
| chr16:89093588-89093696 | Common:3; Rare:31 | ||||
| chr16:89093736-89093976 | Common:5; Rare:104 | ||||
| chr16:89201635-89201970 | Common:2; Rare:117 | ||||
| chr16:89217513-89217780 | Common:1; Rare:132 | ||||
| chr16:89316323-89316643 | Common:2; Rare:63 | ||||
| chr16:89489212-89489514 | Common:6; Rare:116 | ||||
| chr16:89489547-89489618 | Rare:24 | ||||
| chr16:89490318-89490386 | Rare:27 | ||||
| chr16:89490498-89491045 | Common:7; Rare:197 | ||||
| chr16:89491136-89491205 | Rare:21 | ||||
| chr16:89491658-89491832 | Common:1; Rare:38 | ||||
| chr16:89507433-89507702 | Rare:85 | ||||
| chr16:89507801-89507954 | Common:1; Rare:57 |