| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1677985-1678349 | Common:3; Rare:124 | ||||
| chr16:1706086-1706387 | Common:3; Rare:93 | ||||
| chr16:1771484-1771901 | Common:4; Rare:167 | ||||
| chr16:1772606-1772862 | Common:3; Rare:88; Clinvar (pathogenic):2 | ||||
| chr16:1772979-1773254 | Common:2; Rare:105; Clinvar (pathogenic):2 | ||||
| chr16:1773499-1773616 | Rare:49 | ||||
| chr16:1782485-1783023 | Common:4; Rare:187 | ||||
| chr16:1783397-1783504 | Common:1; Rare:31 | ||||
| chr16:1826761-1826975 | Common:3; Rare:72 | ||||
| chr16:1827144-1827232 | Common:1; Rare:38 | ||||
| chr16:1872068-1872327 | Common:8; Rare:110 | ||||
| chr16:1943117-1943554 | Common:1; Rare:138 | ||||
| chr16:1959448-1959753 | Common:5; Rare:142 | ||||
| chr16:1964588-1965085 | Common:17; Rare:224 | ||||
| chr16:1971871-1972131 | Common:3; Rare:78 |