| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70289319-70289849 | Common:5; Rare:189; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:70299068-70299259 | Common:1; Rare:40 | ||||
| chr16:70346508-70346604 | Rare:30 | ||||
| chr16:70346675-70347022 | Common:2; Rare:145 | ||||
| chr16:70347297-70347363 | Rare:10 | ||||
| chr16:70438739-70438763 | Rare:4 | ||||
| chr16:70438946-70439570 | Common:2; Rare:202 | ||||
| chr16:70454049-70454212 | Rare:30 | ||||
| chr16:70454370-70454748 | Common:5; Rare:127 | ||||
| chr16:70523172-70523327 | Common:2; Rare:37 | ||||
| chr16:70523385-70523967 | Common:3; Rare:204; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70523972-70524072 | Rare:23 | ||||
| chr16:70524138-70524213 | Rare:16 | ||||
| chr16:70524583-70524660 | Common:3; Rare:12 | ||||
| chr16:70685428-70685591 | Common:5; Rare:35 |