| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:740924-741131 | Common:1; Rare:71 | ||||
| chr16:760890-761156 | Common:5; Rare:85 | ||||
| chr16:762314-762523 | Rare:50 | ||||
| chr16:1255878-1256079 | Common:1; Rare:45 | ||||
| chr16:1309381-1309727 | Rare:128 | ||||
| chr16:1351868-1351980 | Common:1; Rare:55; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:1414660-1414889 | Common:1; Rare:72 | ||||
| chr16:1420705-1420949 | Common:1; Rare:103 | ||||
| chr16:1493263-1493591 | Common:4; Rare:100 | ||||
| chr16:1533466-1533772 | Common:2; Rare:60 | ||||
| chr16:1706047-1706428 | Common:5; Rare:118 | ||||
| chr16:1771515-1771854 | Common:3; Rare:132 | ||||
| chr16:1772602-1772808 | Common:3; Rare:76; Clinvar (pathogenic):2 | ||||
| chr16:1773126-1773190 | Rare:12 | ||||
| chr16:1782509-1782878 | Common:4; Rare:120 |