| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1773429-1773675 | Common:1; Rare:109 | ||||
| chr16:1782404-1782598 | Common:2; Rare:73 | ||||
| chr16:1782802-1783051 | Rare:87 | ||||
| chr16:1783356-1783414 | Common:2; Rare:19 | ||||
| chr16:1826498-1826634 | Common:3; Rare:40 | ||||
| chr16:1826749-1827005 | Common:4; Rare:86 | ||||
| chr16:1827111-1827530 | Common:3; Rare:202 | ||||
| chr16:1943152-1943568 | Common:1; Rare:128 | ||||
| chr16:1959363-1959630 | Common:6; Rare:110 | ||||
| chr16:1964737-1965137 | Common:18; Rare:182 | ||||
| chr16:1971586-1971727 | Rare:29 | ||||
| chr16:1971770-1972144 | Common:3; Rare:110 | ||||
| chr16:1972581-1972670 | Common:1; Rare:22 | ||||
| chr16:1983498-1983717 | Common:1; Rare:63 | ||||
| chr16:1983863-1984330 | Common:6; Rare:142; Clinvar (benign):4 |