| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:65122998-65123221 | Common:2; Rare:41 | ||||
| chr16:66520850-66521040 | Rare:27 | ||||
| chr16:66557367-66557605 | Rare:31 | ||||
| chr16:66561263-66561445 | Rare:17 | ||||
| chr16:66561930-66562128 | Common:2; Rare:36 | ||||
| chr16:66569183-66569298 | Rare:11 | ||||
| chr16:67395204-67395526 | Rare:79 | ||||
| chr16:67563469-67563800 | Rare:107 | ||||
| chr16:68286286-68286456 | Rare:34 | ||||
| chr16:69324128-69324210 | Common:1; Rare:21 | ||||
| chr16:70042935-70042977 | Rare:3 | ||||
| chr16:70428065-70428333 | Rare:45 | ||||
| chr16:70481009-70481283 | Common:1; Rare:89; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:70664709-70665087 | Rare:183 | ||||
| chr16:70668442-70668679 | Rare:56 |