| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29454320-29454571 | |||||
| chr16:29816110-29816496 | Common:2; Rare:115 | ||||
| chr16:29995604-29995698 | Rare:44 | ||||
| chr16:29996081-29996283 | Common:2; Rare:70 | ||||
| chr16:30064289-30064484 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chr16:30065480-30065841 | Rare:125 | ||||
| chr16:30069659-30069882 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):5 | ||||
| chr16:30075889-30076045 | Rare:51 | ||||
| chr16:30355210-30355434 | Common:1; Rare:78 | ||||
| chr16:30534867-30535081 | Common:2; Rare:73 | ||||
| chr16:30650806-30650960 | Rare:50 | ||||
| chr16:30748109-30748441 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30893942-30894275 | Common:5; Rare:91 | ||||
| chr16:30923257-30923600 | Common:1; Rare:79 | ||||
| chr16:31033458-31033582 | Common:1; Rare:50 |