| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:27203395-27203587 | Rare:64 | ||||
| chr16:27203661-27204060 | Common:5; Rare:136 | ||||
| chr16:27268654-27268910 | Common:1; Rare:92 | ||||
| chr16:27313546-27313677 | Common:2; Rare:38 | ||||
| chr16:27313757-27314007 | Common:5; Rare:69 | ||||
| chr16:27314370-27314668 | Common:1; Rare:59 | ||||
| chr16:27549857-27550230 | Common:2; Rare:150 | ||||
| chr16:28211848-28212378 | Common:5; Rare:172 | ||||
| chr16:28292148-28292628 | Common:2; Rare:114 | ||||
| chr16:28491262-28491471 | Common:1; Rare:53 | ||||
| chr16:28491510-28491559 | Rare:13; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr16:28491938-28492241 | Common:1; Rare:69; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:28492259-28492420 | Common:2; Rare:27; Clinvar (benign):1 | ||||
| chr16:28538969-28539106 | Rare:27 | ||||
| chr16:28553838-28554008 | Common:3; Rare:54 |