| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89217376-89217442 | Common:1; Rare:18 | ||||
| chr16:89217542-89217782 | Common:1; Rare:120 | ||||
| chr16:89489175-89489403 | Common:6; Rare:103 | ||||
| chr16:89490461-89491028 | Common:6; Rare:202 | ||||
| chr16:89507778-89507921 | Common:1; Rare:62 | ||||
| chr16:89508134-89508471 | Common:4; Rare:159; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560428-89560784 | Common:1; Rare:164 | ||||
| chr16:89561376-89561429 | Rare:28 | ||||
| chr16:89575708-89575899 | Common:1; Rare:63 | ||||
| chr16:89657480-89658181 | Common:6; Rare:330; Clinvar (benign):3 | ||||
| chr16:89686645-89686756 | Common:7; Rare:72 | ||||
| chr16:89686858-89687067 | Common:3; Rare:86 | ||||
| chr16:89687260-89687505 | Rare:63 | ||||
| chr16:89701576-89701849 | Common:2; Rare:97 | ||||
| chr16:89702029-89702323 | Common:10; Rare:95 |