| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:23452675-23452808 | Rare:47 | ||||
| chr16:23453150-23453187 | Rare:13 | ||||
| chr16:23557327-23557557 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641219-23641534 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24539864-24540065 | Rare:48 | ||||
| chr16:24729608-24729739 | Common:6; Rare:69 | ||||
| chr16:24804807-24805151 | Rare:77 | ||||
| chr16:25111423-25111821 | Common:2; Rare:105 | ||||
| chr16:27268719-27268875 | Common:1; Rare:54 | ||||
| chr16:27549856-27550190 | Common:2; Rare:134 | ||||
| chr16:28494471-28494684 | Rare:51 | ||||
| chr16:28595629-28595902 | Common:3; Rare:114 | ||||
| chr16:28596984-28597226 | Common:3; Rare:67 | ||||
| chr16:28822587-28822752 | Rare:65 | ||||
| chr16:28822931-28823033 | Common:2; Rare:30 |