| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70671443-70671448 | |||||
| chr16:70680784-70680952 | Common:2; Rare:62 | ||||
| chr16:71733116-71733383 | Common:1; Rare:48 | ||||
| chr16:72107506-72107713 | Rare:74 | ||||
| chr16:72664927-72665208 | Common:2; Rare:91 | ||||
| chr16:74302053-74302292 | Common:1; Rare:57 | ||||
| chr16:74319246-74319324 | Rare:11 | ||||
| chr16:74368115-74368376 | Common:1; Rare:75 | ||||
| chr16:74691969-74692024 | Rare:13 | ||||
| chr16:75567878-75568096 | Common:1; Rare:68 | ||||
| chr16:79505370-79505627 | Common:4; Rare:72 | ||||
| chr16:79597809-79598063 | Common:3; Rare:60 | ||||
| chr16:79598316-79598671 | Common:11; Rare:73 | ||||
| chr16:79598831-79598986 | Rare:40; Clinvar (benign):1 | ||||
| chr16:79770559-79770726 | Common:5; Rare:75 |