| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:78111-78300 | Common:3; Rare:66 | ||||
| chr16:229041-229186 | Common:2; Rare:69 | ||||
| chr16:234727-234868 | Rare:63 | ||||
| chr16:254000-254133 | Common:1; Rare:21 | ||||
| chr16:275889-275944 | Rare:13 | ||||
| chr16:376779-377062 | Common:3; Rare:87 | ||||
| chr16:396969-397297 | Common:8; Rare:79 | ||||
| chr16:401716-402013 | Common:2; Rare:126 | ||||
| chr16:502537-502961 | Common:5; Rare:83 | ||||
| chr16:636190-636457 | Common:4; Rare:80 | ||||
| chr16:641744-641956 | Common:3; Rare:73 | ||||
| chr16:655604-655816 | Common:1; Rare:88 | ||||
| chr16:672104-672376 | Common:4; Rare:133 | ||||
| chr16:680339-680479 | Common:2; Rare:49 | ||||
| chr16:681141-681544 | Rare:128; Clinvar:1; Clinvar (pathogenic):5 |