| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:7332684-7332987 | Common:1; Rare:97 | ||||
| chr16:8797621-8797877 | Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:8841957-8842304 | Common:14; Rare:87 | ||||
| chr16:8868973-8869248 | Common:4; Rare:124 | ||||
| chr16:10385859-10386101 | Rare:88 | ||||
| chr16:10580558-10580867 | Common:2; Rare:102 | ||||
| chr16:10743702-10743891 | Rare:79 | ||||
| chr16:10944333-10944646 | Common:1; Rare:99 | ||||
| chr16:11586891-11587028 | Common:1; Rare:40 | ||||
| chr16:11851499-11851645 | Rare:71 | ||||
| chr16:11915895-11916229 | Common:2; Rare:134 | ||||
| chr16:11976604-11976777 | Common:3; Rare:75 | ||||
| chr16:14071065-14071360 | Common:1; Rare:104 | ||||
| chr16:14630188-14630393 | Rare:93 | ||||
| chr16:14632729-14632981 | Common:1; Rare:84 |