| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1772249-1772547 | Common:1; Rare:148 | ||||
| chr16:1772573-1772837 | Common:3; Rare:100; Clinvar (pathogenic):2 | ||||
| chr16:1773060-1773230 | Rare:59; Clinvar (pathogenic):1 | ||||
| chr16:1773482-1773602 | Rare:47 | ||||
| chr16:1782489-1782642 | Common:3; Rare:64 | ||||
| chr16:1782788-1783058 | Rare:96 | ||||
| chr16:1783665-1783696 | Common:1; Rare:6 | ||||
| chr16:1826508-1826640 | Common:3; Rare:37 | ||||
| chr16:1826772-1826982 | Common:3; Rare:67 | ||||
| chr16:1827144-1827329 | Common:1; Rare:91 | ||||
| chr16:1872054-1872327 | Common:9; Rare:116 | ||||
| chr16:1943152-1943551 | Common:1; Rare:125 | ||||
| chr16:1959363-1959604 | Common:6; Rare:95 | ||||
| chr16:1963081-1963126 | Common:1; Rare:22 | ||||
| chr16:1964699-1965203 | Common:18; Rare:227 |