| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29996069-29996317 | Common:2; Rare:91 | ||||
| chr16:30064338-30064482 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chr16:30065562-30065923 | Rare:124 | ||||
| chr16:30069490-30070038 | Common:1; Rare:202; Clinvar:6; Clinvar (benign):7 | ||||
| chr16:30075894-30076055 | Rare:55 | ||||
| chr16:30113343-30113660 | Common:1; Rare:82 | ||||
| chr16:30117729-30117964 | Common:1; Rare:43 | ||||
| chr16:30123013-30123378 | Common:6; Rare:107 | ||||
| chr16:30184533-30184668 | Common:1; Rare:23 | ||||
| chr16:30193654-30193953 | |||||
| chr16:30355210-30355453 | Common:2; Rare:84 | ||||
| chr16:30355846-30355969 | Common:1; Rare:27 | ||||
| chr16:30407457-30407637 | Rare:63 | ||||
| chr16:30445828-30446050 | Common:1; Rare:65 | ||||
| chr16:30472570-30472741 | Rare:32 |