| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69718121-69718531 | Common:1; Rare:113 | ||||
| chr16:70042951-70042989 | Rare:3 | ||||
| chr16:70188230-70188322 | Common:2; Rare:23 | ||||
| chr16:71896176-71896221 | Common:1; Rare:14 | ||||
| chr16:72664962-72665182 | Rare:74 | ||||
| chr16:73070577-73070736 | Common:1; Rare:44 | ||||
| chr16:74302018-74302292 | Common:1; Rare:64 | ||||
| chr16:74368122-74368386 | Common:1; Rare:73 | ||||
| chr16:74407187-74407275 | Common:2; Rare:17 | ||||
| chr16:77761166-77761505 | Common:1; Rare:58 | ||||
| chr16:79597672-79597968 | Common:2; Rare:62 | ||||
| chr16:79598529-79599105 | Common:9; Rare:148; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:79770327-79770470 | Common:2; Rare:44 | ||||
| chr16:79770501-79770726 | Common:5; Rare:97 | ||||
| chr16:81669801-81669979 | Common:2; Rare:51 |