| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56989458-56989605 | Common:1; Rare:31; Clinvar:1 | ||||
| chr16:57185804-57186371 | Common:3; Rare:159 | ||||
| chr16:57244956-57245323 | Common:3; Rare:123 | ||||
| chr16:57447354-57447508 | Common:2; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:57629220-57629339 | Common:3; Rare:22 | ||||
| chr16:57803209-57803423 | Rare:39 | ||||
| chr16:58001310-58001463 | Rare:44 | ||||
| chr16:58129295-58129576 | Common:3; Rare:90 | ||||
| chr16:58249854-58250017 | Rare:46 | ||||
| chr16:58392783-58392859 | Common:2; Rare:21 | ||||
| chr16:58629763-58630141 | Common:2; Rare:104 | ||||
| chr16:58684704-58684857 | Common:1; Rare:44 | ||||
| chr16:58734234-58734391 | Common:4; Rare:50 | ||||
| chr16:66516819-66517065 | Rare:40 | ||||
| chr16:66552461-66552739 | Rare:112 |