| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71564700-71564902 | Common:1; Rare:45 | ||||
| chr16:71564916-71565259 | Common:2; Rare:97 | ||||
| chr16:71565588-71565733 | Common:1; Rare:27 | ||||
| chr16:71723579-71723652 | Rare:17 | ||||
| chr16:71723821-71724081 | Common:5; Rare:91 | ||||
| chr16:71808315-71808460 | Rare:52 | ||||
| chr16:71808552-71809394 | Common:4; Rare:327 | ||||
| chr16:71809516-71809589 | Rare:21 | ||||
| chr16:71809596-71809679 | Rare:10 | ||||
| chr16:71845791-71846074 | Common:2; Rare:93 | ||||
| chr16:71884054-71884339 | Common:1; Rare:95 | ||||
| chr16:71894348-71894466 | Rare:30 | ||||
| chr16:71895137-71895631 | Common:4; Rare:192 | ||||
| chr16:72008457-72008876 | Common:6; Rare:171; Clinvar (benign):2 | ||||
| chr16:72093508-72094016 | Common:1; Rare:125 |