| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4670622-4670646 | Common:1; Rare:6 | ||||
| chr16:4797860-4797981 | Common:1; Rare:69; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:4901718-4902006 | Common:11; Rare:70 | ||||
| chr16:5061507-5061679 | Common:4; Rare:30 | ||||
| chr16:6882511-6882525 | Rare:5 | ||||
| chr16:7768458-7768744 | Common:2; Rare:68 | ||||
| chr16:8804449-8804844 | Common:3; Rare:94; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr16:8814794-8814806 | Rare:3 | ||||
| chr16:8828053-8828214 | Common:3; Rare:18 | ||||
| chr16:8839278-8839579 | Rare:82 | ||||
| chr16:8862348-8862364 | Rare:5 | ||||
| chr16:8894662-8894838 | Common:3; Rare:50 | ||||
| chr16:8894846-8895139 | Common:1; Rare:92 | ||||
| chr16:8916794-8916961 | Common:1; Rare:41 | ||||
| chr16:8954786-8954827 | Rare:13 |