| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67430855-67431641 | Common:10; Rare:324; Clinvar (pathogenic):2 | ||||
| chr16:67481062-67481447 | Common:5; Rare:395 | ||||
| chr16:67528691-67528950 | Rare:143 | ||||
| chr16:67529030-67529380 | Rare:94 | ||||
| chr16:67537578-67538555 | Common:10; Rare:336 | ||||
| chr16:67561931-67562719 | Common:3; Rare:572 | ||||
| chr16:67660160-67660426 | Rare:404; Clinvar:8; Clinvar (benign):6 | ||||
| chr16:67660719-67661079 | Common:6; Rare:251 | ||||
| chr16:67719221-67719541 | Common:3; Rare:237 | ||||
| chr16:67806400-67806940 | Rare:336 | ||||
| chr16:67833830-67834016 | Common:1; Rare:73 | ||||
| chr16:67841827-67842166 | Common:6; Rare:260 | ||||
| chr16:67842190-67842460 | Common:1; Rare:191 | ||||
| chr16:67846316-67847325 | Common:9; Rare:561 | ||||
| chr16:67847601-67848432 | Common:6; Rare:252 |