| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:18801529-18801831 | Common:4; Rare:93 | ||||
| chr16:23641278-23641525 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23678716-23678935 | Common:4; Rare:67 | ||||
| chr16:24729534-24729730 | Common:6; Rare:95 | ||||
| chr16:25111490-25111762 | Common:2; Rare:65 | ||||
| chr16:27268724-27268872 | Common:1; Rare:50 | ||||
| chr16:27549892-27550161 | Common:2; Rare:95 | ||||
| chr16:28822600-28822761 | Rare:66 | ||||
| chr16:28925173-28925365 | Rare:58 | ||||
| chr16:29454097-29454571 | |||||
| chr16:29816002-29816220 | Common:1; Rare:63 | ||||
| chr16:29816325-29816521 | Common:1; Rare:65 | ||||
| chr16:29995601-29995696 | Rare:45 | ||||
| chr16:29996154-29996296 | Common:1; Rare:54 | ||||
| chr16:30075905-30076045 | Rare:49 |