| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:57803312-57803541 | Common:1; Rare:39 | ||||
| chr16:58001280-58001637 | Common:2; Rare:123; Clinvar (benign):1 | ||||
| chr16:58129246-58129581 | Common:4; Rare:105 | ||||
| chr16:58249859-58250033 | Rare:50 | ||||
| chr16:58392787-58392891 | Common:2; Rare:27 | ||||
| chr16:58515408-58515549 | Common:2; Rare:56 | ||||
| chr16:58629738-58630139 | Common:2; Rare:111 | ||||
| chr16:58684711-58684831 | Rare:37 | ||||
| chr16:58734149-58734449 | Common:5; Rare:87 | ||||
| chr16:65121944-65122356 | Common:1; Rare:132 | ||||
| chr16:65123802-65123942 | Common:1; Rare:36 | ||||
| chr16:65124477-65124557 | Rare:11 | ||||
| chr16:65125770-65126261 | Common:2; Rare:87 | ||||
| chr16:66516808-66517106 | Rare:48 | ||||
| chr16:66549813-66550037 | Common:1; Rare:93; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |