| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:55478817-55478977 | Rare:29 | ||||
| chr16:55479143-55479484 | Common:2; Rare:98; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:55509562-55509948 | Common:2; Rare:67 | ||||
| chr16:56451149-56451674 | Common:4; Rare:175 | ||||
| chr16:56608510-56608770 | Common:2; Rare:78 | ||||
| chr16:56729988-56730185 | Common:1; Rare:44 | ||||
| chr16:56989381-56989593 | Common:1; Rare:50; Clinvar:1 | ||||
| chr16:57185956-57186365 | Common:1; Rare:123 | ||||
| chr16:57447355-57447508 | Common:2; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:58129311-58129548 | Common:2; Rare:76 | ||||
| chr16:66366493-66366707 | Common:2; Rare:45 | ||||
| chr16:66552480-66552632 | Rare:65 | ||||
| chr16:66934365-66934528 | Rare:60 | ||||
| chr16:67159870-67159920 | Rare:7 | ||||
| chr16:67226846-67227187 | Common:1; Rare:124 |