| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:57185724-57186438 | Common:4; Rare:200 | ||||
| chr16:57244982-57245283 | Common:3; Rare:95 | ||||
| chr16:57447348-57447514 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:57628175-57628406 | Common:1; Rare:50 | ||||
| chr16:57628501-57628715 | Common:3; Rare:53 | ||||
| chr16:57639366-57639647 | Common:2; Rare:49; Clinvar (pathogenic):1 | ||||
| chr16:57984908-57985176 | Common:5; Rare:81 | ||||
| chr16:58001318-58001472 | Rare:46 | ||||
| chr16:58129232-58129540 | Common:2; Rare:95 | ||||
| chr16:58249825-58250096 | Rare:79 | ||||
| chr16:58463794-58464064 | Rare:70 | ||||
| chr16:58629778-58630121 | Common:2; Rare:90 | ||||
| chr16:58684697-58684818 | Rare:36 | ||||
| chr16:58734229-58734426 | Common:4; Rare:58 | ||||
| chr16:62036254-62036625 | Rare:85 |