| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:690350-690459 | Common:1; Rare:52 | ||||
| chr16:740944-741141 | Rare:67 | ||||
| chr16:970826-971143 | Common:7; Rare:147 | ||||
| chr16:1230173-1230488 | Common:1; Rare:66 | ||||
| chr16:1309354-1309727 | Rare:139 | ||||
| chr16:1333525-1333665 | Common:1; Rare:65 | ||||
| chr16:1351879-1352002 | Common:1; Rare:67; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:1420707-1420938 | Common:1; Rare:96 | ||||
| chr16:1444506-1444595 | Common:1; Rare:21 | ||||
| chr16:1493228-1493587 | Common:4; Rare:106 | ||||
| chr16:1528490-1528743 | Common:2; Rare:84 | ||||
| chr16:1533494-1533694 | Common:1; Rare:39 | ||||
| chr16:1611987-1612376 | Common:2; Rare:138; Clinvar:2 | ||||
| chr16:1631988-1632296 | Common:1; Rare:71 | ||||
| chr16:1678004-1678321 | Common:3; Rare:106 |