| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1309402-1309773 | Rare:137 | ||||
| chr16:1414679-1414889 | Common:1; Rare:61 | ||||
| chr16:1420705-1420943 | Common:1; Rare:98 | ||||
| chr16:1493263-1493598 | Common:4; Rare:101 | ||||
| chr16:1612042-1612385 | Common:2; Rare:122; Clinvar:1 | ||||
| chr16:1677997-1678349 | Common:3; Rare:120 | ||||
| chr16:1706021-1706445 | Common:5; Rare:138 | ||||
| chr16:1771502-1771869 | Common:3; Rare:144 | ||||
| chr16:1773047-1773212 | Common:1; Rare:56; Clinvar (pathogenic):1 | ||||
| chr16:1782507-1783015 | Common:4; Rare:168 | ||||
| chr16:1826785-1826982 | Common:3; Rare:62 | ||||
| chr16:1827171-1827445 | Common:2; Rare:153 | ||||
| chr16:1943152-1943497 | Common:1; Rare:107 | ||||
| chr16:1959407-1959714 | Common:6; Rare:133 | ||||
| chr16:1964817-1965075 | Common:7; Rare:109 |