| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:66877966-66878366 | Common:1; Rare:59 | ||||
| chr16:66880250-66880660 | Common:8; Rare:312 | ||||
| chr16:66934020-66934270 | Common:1; Rare:84 | ||||
| chr16:66934269-66934669 | Common:6; Rare:528 | ||||
| chr16:66934762-66935347 | Common:1; Rare:174 | ||||
| chr16:66961125-66961305 | Common:2; Rare:42 | ||||
| chr16:67028329-67028767 | Common:3; Rare:121 | ||||
| chr16:67028809-67030127 | Common:20; Rare:1414 | ||||
| chr16:67109286-67110082 | Common:4; Rare:698 | ||||
| chr16:67150777-67151489 | Common:4; Rare:362 | ||||
| chr16:67158974-67159640 | Rare:255 | ||||
| chr16:67159680-67160039 | Rare:204 | ||||
| chr16:67160060-67160925 | Rare:236 | ||||
| chr16:67160857-67161257 | Common:3; Rare:277 | ||||
| chr16:67164496-67164896 | Common:1; Rare:214; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 |