| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75148391-75148596 | Common:4; Rare:93 | ||||
| chr16:75305306-75305747 | Common:2; Rare:80 | ||||
| chr16:75433402-75433875 | Common:4; Rare:148 | ||||
| chr16:75464380-75464448 | Common:2; Rare:28 | ||||
| chr16:75556214-75556354 | Common:1; Rare:49; Clinvar (benign):3 | ||||
| chr16:75623214-75623416 | Common:3; Rare:75 | ||||
| chr16:75647605-75647846 | Common:3; Rare:119; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190696-77191010 | Common:10; Rare:103 | ||||
| chr16:77191139-77191214 | Common:1; Rare:34 | ||||
| chr16:78099308-78099632 | Common:2; Rare:113 | ||||
| chr16:79600721-79600970 | Common:1; Rare:68 | ||||
| chr16:81006442-81006562 | Rare:37 | ||||
| chr16:81006774-81006974 | Common:4; Rare:84 | ||||
| chr16:81007120-81007301 | Common:1; Rare:54 | ||||
| chr16:81007496-81007688 | Common:6; Rare:63 |