| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:20763937-20764026 | Common:2; Rare:14 | ||||
| chr16:20806349-20806533 | Rare:69 | ||||
| chr16:20900322-20900819 | Common:3; Rare:113 | ||||
| chr16:21953038-21953419 | Common:1; Rare:97; Clinvar (benign):3 | ||||
| chr16:22437189-22437313 | Rare:37 | ||||
| chr16:22437518-22437676 | Common:2; Rare:40 | ||||
| chr16:23557348-23557650 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641223-23641525 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678665-23678947 | Common:5; Rare:86 | ||||
| chr16:24729604-24729734 | Common:6; Rare:70 | ||||
| chr16:25111520-25111803 | Common:2; Rare:84 | ||||
| chr16:27268724-27268851 | Common:1; Rare:40 | ||||
| chr16:27549877-27550161 | Common:2; Rare:105 | ||||
| chr16:28846271-28846623 | Common:2; Rare:121; Clinvar:5; Clinvar (benign):5 | ||||
| chr16:28974682-28974792 | Rare:51 |