| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56608520-56608906 | Common:2; Rare:101 | ||||
| chr16:56608913-56609065 | Rare:49 | ||||
| chr16:56625708-56626063 | Rare:99 | ||||
| chr16:56682418-56682571 | Common:3; Rare:65 | ||||
| chr16:56729770-56730202 | Common:2; Rare:92 | ||||
| chr16:56931923-56932181 | Common:2; Rare:133 | ||||
| chr16:56935058-56935476 | Common:2; Rare:105 | ||||
| chr16:56989373-56989605 | Common:1; Rare:55; Clinvar:1 | ||||
| chr16:57092589-57092630 | Rare:11 | ||||
| chr16:57185736-57186468 | Common:5; Rare:204 | ||||
| chr16:57245218-57245397 | Rare:60 | ||||
| chr16:57447342-57447549 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:57619968-57620150 | Rare:42 | ||||
| chr16:57735655-57735868 | Common:1; Rare:48 | ||||
| chr16:57764336-57764423 | Rare:16 |