| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74297483-74297779 | Common:2; Rare:57 | ||||
| chr16:74314235-74314275 | Common:1; Rare:10 | ||||
| chr16:75517255-75517373 | Rare:48 | ||||
| chr16:75520621-75520735 | Rare:18 | ||||
| chr16:77971604-77971892 | Common:2; Rare:100 | ||||
| chr16:78314281-78314509 | Common:6; Rare:56 | ||||
| chr16:79598292-79598571 | Common:4; Rare:52 | ||||
| chr16:79598895-79599041 | Rare:32; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:79770291-79770434 | Common:2; Rare:52 | ||||
| chr16:81141558-81141617 | Rare:25 | ||||
| chr16:81729265-81729621 | Common:6; Rare:80 | ||||
| chr16:82663229-82663341 | Common:2; Rare:43 | ||||
| chr16:84618679-84618827 | Common:1; Rare:36 | ||||
| chr16:85555347-85555527 | Rare:45 | ||||
| chr16:85555894-85556156 | Common:1; Rare:65 |