| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58734234-58734391 | Common:4; Rare:50 | ||||
| chr16:62036424-62036597 | Rare:43 | ||||
| chr16:65121920-65122169 | Common:1; Rare:97 | ||||
| chr16:66552473-66552718 | Rare:102 | ||||
| chr16:66880352-66880608 | Common:2; Rare:64 | ||||
| chr16:66934356-66934506 | Common:1; Rare:55 | ||||
| chr16:67028944-67029116 | Rare:68 | ||||
| chr16:67109819-67110002 | Rare:59 | ||||
| chr16:67159880-67160018 | Rare:23 | ||||
| chr16:67227008-67227201 | Rare:83 | ||||
| chr16:67277990-67278201 | Rare:40 | ||||
| chr16:67393475-67393796 | Common:1; Rare:70 | ||||
| chr16:67481091-67481378 | Common:1; Rare:107 | ||||
| chr16:67528671-67528883 | Rare:58 | ||||
| chr16:67660224-67660360 | Rare:79; Clinvar:2; Clinvar (benign):2 |