| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67968577-67968928 | Common:2; Rare:106 | ||||
| chr16:68023190-68023318 | Common:2; Rare:40 | ||||
| chr16:68084741-68084819 | Rare:14 | ||||
| chr16:68237559-68237887 | Rare:91 | ||||
| chr16:68245161-68245410 | Common:1; Rare:74 | ||||
| chr16:68264427-68264661 | Rare:70 | ||||
| chr16:68265278-68265475 | Rare:28 | ||||
| chr16:68265578-68265622 | Common:1; Rare:7 | ||||
| chr16:68310858-68311144 | Common:3; Rare:145 | ||||
| chr16:68530049-68530139 | Common:4; Rare:42 | ||||
| chr16:68539156-68539344 | Common:2; Rare:89 | ||||
| chr16:68843231-68843618 | Rare:87 | ||||
| chr16:69132504-69132686 | Rare:67 | ||||
| chr16:69311096-69311503 | Rare:125 | ||||
| chr16:69339548-69339832 | Common:1; Rare:121; Clinvar (benign):1 |