| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1493143-1493609 | Common:5; Rare:133 | ||||
| chr16:1493778-1493828 | Rare:6 | ||||
| chr16:1610160-1610472 | Common:2; Rare:73 | ||||
| chr16:1610598-1610892 | Common:1; Rare:98; Clinvar:1 | ||||
| chr16:1610991-1611073 | Rare:18 | ||||
| chr16:1611952-1612515 | Common:6; Rare:212; Clinvar:2 | ||||
| chr16:1614031-1614349 | Common:3; Rare:77 | ||||
| chr16:1614375-1614585 | Rare:57 | ||||
| chr16:1678066-1678492 | Common:3; Rare:130 | ||||
| chr16:1678496-1678545 | Rare:15 | ||||
| chr16:1678675-1678777 | Common:3; Rare:27 | ||||
| chr16:1705808-1706395 | Common:5; Rare:172 | ||||
| chr16:1772414-1772516 | Common:1; Rare:40 | ||||
| chr16:1772573-1772920 | Common:3; Rare:122; Clinvar (pathogenic):2 | ||||
| chr16:1773055-1773254 | Rare:76; Clinvar (pathogenic):1 |