| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29995605-29995708 | Rare:46 | ||||
| chr16:29996073-29996296 | Common:2; Rare:78 | ||||
| chr16:30010957-30011111 | Rare:38 | ||||
| chr16:30064088-30064497 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr16:30065548-30065835 | Rare:104 | ||||
| chr16:30069660-30070018 | Common:1; Rare:124; Clinvar:3; Clinvar (benign):7 | ||||
| chr16:30075889-30076045 | Rare:51 | ||||
| chr16:30123064-30123367 | Common:6; Rare:84 | ||||
| chr16:30355219-30355442 | Common:1; Rare:81 | ||||
| chr16:30527296-30527596 | Common:1; Rare:81 | ||||
| chr16:30534822-30535095 | Common:3; Rare:85 | ||||
| chr16:30571558-30571755 | Rare:57 | ||||
| chr16:30585570-30585902 | Common:1; Rare:69 | ||||
| chr16:30698019-30698235 | Common:1; Rare:105 | ||||
| chr16:30698457-30698639 | Common:1; Rare:69 |