| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:24729597-24729789 | Common:7; Rare:87 | ||||
| chr16:25015291-25015433 | Common:1; Rare:55 | ||||
| chr16:25111478-25111797 | Common:2; Rare:82 | ||||
| chr16:27268713-27268872 | Common:1; Rare:57 | ||||
| chr16:27549856-27550177 | Common:2; Rare:129 | ||||
| chr16:28538768-28539122 | Common:2; Rare:99 | ||||
| chr16:28554165-28554439 | Common:4; Rare:90 | ||||
| chr16:28822706-28822734 | Rare:11 | ||||
| chr16:28823964-28824091 | Rare:33 | ||||
| chr16:28824284-28824469 | Common:2; Rare:63 | ||||
| chr16:28843806-28844127 | Rare:109; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr16:28846256-28846715 | Common:2; Rare:151; Clinvar:6; Clinvar (benign):6 | ||||
| chr16:28863494-28863992 | Common:3; Rare:124 | ||||
| chr16:28925172-28925405 | Rare:77 | ||||
| chr16:28925682-28925816 | Rare:23 |