| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1474391-1474652 | Common:2; Rare:79 | ||||
| chr16:1474899-1475326 | Common:6; Rare:139; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:1475374-1475537 | Common:3; Rare:33 | ||||
| chr16:1492987-1493634 | Common:5; Rare:175 | ||||
| chr16:1493774-1493824 | Rare:7 | ||||
| chr16:1610019-1610107 | Rare:26 | ||||
| chr16:1610184-1610320 | Common:2; Rare:29 | ||||
| chr16:1610325-1610516 | Rare:51 | ||||
| chr16:1610578-1610923 | Common:1; Rare:112; Clinvar:1 | ||||
| chr16:1610960-1611198 | Rare:46 | ||||
| chr16:1611944-1612569 | Common:6; Rare:228; Clinvar:2 | ||||
| chr16:1612818-1612994 | Common:1; Rare:59 | ||||
| chr16:1614118-1614360 | Common:1; Rare:69 | ||||
| chr16:1614373-1614684 | Rare:74 | ||||
| chr16:1614921-1614968 | Common:1; Rare:12 |