| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46689512-46689708 | Common:2; Rare:83; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973537-46973753 | Rare:86 | ||||
| chr16:47460884-47461383 | Common:2; Rare:204; Clinvar (benign):2 | ||||
| chr16:48244248-48244559 | Common:2; Rare:93 | ||||
| chr16:53054720-53055048 | Common:2; Rare:73 | ||||
| chr16:53703821-53704215 | Common:1; Rare:125; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54286705-54287030 | Common:2; Rare:98 | ||||
| chr16:56451280-56451605 | Common:1; Rare:104 | ||||
| chr16:56519973-56520177 | Common:4; Rare:71; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:56625476-56625877 | Common:1; Rare:116 | ||||
| chr16:56632276-56632574 | Common:2; Rare:81 | ||||
| chr16:56729941-56730202 | Common:1; Rare:63 | ||||
| chr16:56931915-56932283 | Common:3; Rare:187 | ||||
| chr16:56989458-56989602 | Common:1; Rare:30; Clinvar:1 | ||||
| chr16:57185997-57186391 | Common:1; Rare:125 |