| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:15897898-15898015 | Rare:15 | ||||
| chr16:15899710-15899897 | Rare:29 | ||||
| chr16:15948889-15949026 | Rare:21 | ||||
| chr16:15950484-15950593 | Common:1; Rare:22 | ||||
| chr16:15998629-15998676 | Rare:10 | ||||
| chr16:16007138-16007363 | Common:8; Rare:57 | ||||
| chr16:16007805-16008095 | Common:1; Rare:91 | ||||
| chr16:17013689-17013805 | Common:1; Rare:25 | ||||
| chr16:17023405-17023522 | Rare:25 | ||||
| chr16:17026890-17027042 | Common:2; Rare:30 | ||||
| chr16:17027820-17027962 | Common:1; Rare:19 | ||||
| chr16:17068667-17068818 | Rare:30 | ||||
| chr16:17070774-17071194 | Common:2; Rare:91 | ||||
| chr16:17076457-17076617 | Common:1; Rare:33 | ||||
| chr16:17134655-17134780 | Rare:44; Clinvar:1; Clinvar (pathogenic):1 |