| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:23557327-23557419 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641247-23641530 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678725-23678947 | Common:4; Rare:70 | ||||
| chr16:24539344-24539612 | Common:1; Rare:94 | ||||
| chr16:24729604-24729730 | Common:6; Rare:69 | ||||
| chr16:25111508-25111843 | Common:2; Rare:100 | ||||
| chr16:27203407-27203526 | Rare:30 | ||||
| chr16:27268719-27268872 | Common:1; Rare:52 | ||||
| chr16:27549850-27550167 | Common:2; Rare:123 | ||||
| chr16:28822529-28822749 | Common:1; Rare:77 | ||||
| chr16:28846289-28846618 | Common:2; Rare:113; Clinvar:5; Clinvar (benign):4 | ||||
| chr16:28879866-28880098 | Common:3; Rare:73 | ||||
| chr16:28925212-28925277 | Rare:16 | ||||
| chr16:28974669-28974792 | Rare:56 | ||||
| chr16:29790431-29790757 | Common:1; Rare:106 |