| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29996072-29996296 | Common:2; Rare:79 | ||||
| chr16:30065575-30065921 | Rare:117 | ||||
| chr16:30069495-30070022 | Common:1; Rare:197; Clinvar:6; Clinvar (benign):7 | ||||
| chr16:30075900-30076055 | Rare:54 | ||||
| chr16:30184528-30184726 | Common:1; Rare:34 | ||||
| chr16:30355212-30355434 | Common:1; Rare:77 | ||||
| chr16:30534835-30535082 | Common:2; Rare:81 | ||||
| chr16:30585537-30585902 | Common:1; Rare:82 | ||||
| chr16:30698455-30698658 | Common:1; Rare:79 | ||||
| chr16:30699052-30699370 | Rare:79; Clinvar (benign):1 | ||||
| chr16:30762093-30762344 | Common:3; Rare:85 | ||||
| chr16:30893940-30894206 | Common:4; Rare:67 | ||||
| chr16:30923256-30923592 | Common:1; Rare:81 | ||||
| chr16:31033227-31033777 | Common:2; Rare:149 | ||||
| chr16:31074187-31074450 | Common:1; Rare:73 |