| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89150182-89150386 | Rare:38 | ||||
| chr16:89201674-89201997 | Common:4; Rare:105 | ||||
| chr16:89217045-89217442 | Common:3; Rare:103 | ||||
| chr16:89217518-89217789 | Common:1; Rare:133 | ||||
| chr16:89489218-89489516 | Common:4; Rare:108 | ||||
| chr16:89489555-89489635 | Rare:28 | ||||
| chr16:89490303-89490398 | Rare:35 | ||||
| chr16:89490503-89491043 | Common:7; Rare:195 | ||||
| chr16:89491082-89491209 | Common:1; Rare:37 | ||||
| chr16:89491662-89491683 | Rare:5 | ||||
| chr16:89507530-89507698 | Rare:63 | ||||
| chr16:89507705-89507931 | Common:3; Rare:106 | ||||
| chr16:89507951-89508088 | Rare:40 | ||||
| chr16:89508211-89508694 | Common:3; Rare:225; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr16:89508822-89508928 | Rare:58 |