| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:15784648-15784758 | Rare:38; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:15789078-15789155 | Rare:4 | ||||
| chr16:15798657-15798717 | Common:1; Rare:29; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:15854887-15855152 | Common:3; Rare:52 | ||||
| chr16:17469206-17469341 | Rare:21 | ||||
| chr16:21820388-21820471 | Rare:18 | ||||
| chr16:27327011-27327076 | Rare:18 | ||||
| chr16:27330581-27330848 | Common:2; Rare:52 | ||||
| chr16:29139559-29139701 | Common:2; Rare:29 | ||||
| chr16:29595046-29595113 | Common:5; Rare:45 | ||||
| chr16:30335289-30335541 | Common:2; Rare:93 | ||||
| chr16:30634283-30634559 | Common:1; Rare:71 | ||||
| chr16:30875350-30875465 | Rare:36 | ||||
| chr16:50323632-50323749 | Common:1; Rare:22 | ||||
| chr16:53470625-53470922 | Common:1; Rare:66 |