| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:20900226-20900792 | Common:3; Rare:126 | ||||
| chr16:21158547-21158735 | Common:1; Rare:56 | ||||
| chr16:21652602-21652629 | Rare:12 | ||||
| chr16:21953000-21953435 | Common:1; Rare:109; Clinvar (benign):3 | ||||
| chr16:22436942-22437086 | Rare:55 | ||||
| chr16:22437166-22437319 | Rare:46 | ||||
| chr16:23453118-23453242 | Rare:36 | ||||
| chr16:23557336-23557594 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641223-23641536 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24729604-24729766 | Common:7; Rare:81 | ||||
| chr16:25111521-25111805 | Common:2; Rare:83 | ||||
| chr16:27268724-27268872 | Common:1; Rare:50 | ||||
| chr16:27313767-27313985 | Common:5; Rare:63 | ||||
| chr16:27549865-27550173 | Common:2; Rare:122 | ||||
| chr16:28538815-28539165 | Common:2; Rare:83 |