| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46689518-46689708 | Common:2; Rare:79; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973626-46973753 | Rare:60 | ||||
| chr16:47460986-47461374 | Common:2; Rare:158; Clinvar (benign):2 | ||||
| chr16:52547480-52547499 | Rare:5 | ||||
| chr16:53703813-53704215 | Common:1; Rare:127; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:56191063-56191418 | Common:6; Rare:126 | ||||
| chr16:56191603-56191713 | Rare:20 | ||||
| chr16:56191723-56191857 | Common:1; Rare:45 | ||||
| chr16:56192154-56192279 | Rare:31; Clinvar (benign):2 | ||||
| chr16:56451296-56451600 | Common:1; Rare:96 | ||||
| chr16:56519973-56520133 | Common:4; Rare:61; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:56608440-56608658 | Common:2; Rare:64 | ||||
| chr16:56657581-56658040 | Common:3; Rare:122 | ||||
| chr16:56729947-56730189 | Common:1; Rare:58 | ||||
| chr16:56781542-56781875 | Common:1; Rare:58 |