| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1474944-1475164 | Common:3; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:1533462-1533707 | Common:2; Rare:49 | ||||
| chr16:1612029-1612435 | Common:3; Rare:145; Clinvar:1 | ||||
| chr16:1706043-1706438 | Common:5; Rare:125 | ||||
| chr16:1768366-1768623 | Common:1; Rare:103 | ||||
| chr16:1771484-1771868 | Common:3; Rare:154 | ||||
| chr16:1772659-1772898 | Common:2; Rare:75; Clinvar (pathogenic):1 | ||||
| chr16:1773050-1773235 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
| chr16:1773333-1773617 | Common:2; Rare:120 | ||||
| chr16:1781711-1781809 | Rare:22 | ||||
| chr16:1782490-1783023 | Common:4; Rare:184 | ||||
| chr16:1826770-1826975 | Common:3; Rare:68 | ||||
| chr16:1827149-1827515 | Common:3; Rare:185 | ||||
| chr16:1943117-1943535 | Common:1; Rare:133 | ||||
| chr16:1959492-1959753 | Common:4; Rare:121 |