| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:37899483-37899742 | Common:3; Rare:102 | ||||
| chr8:38176426-38176890 | Common:6; Rare:135 | ||||
| chr8:38269125-38269313 | Rare:73 | ||||
| chr8:38386346-38386514 | Rare:35 | ||||
| chr8:38786959-38787253 | Rare:106 | ||||
| chr8:38787973-38788034 | Rare:11 | ||||
| chr8:41490218-41490479 | Rare:59 | ||||
| chr8:41577938-41578256 | Rare:99 | ||||
| chr8:42051975-42052272 | Common:1; Rare:86 | ||||
| chr8:42541554-42541661 | Rare:34 | ||||
| chr8:42541678-42542045 | Common:1; Rare:113; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:42843046-42843089 | Rare:11; Clinvar:2 | ||||
| chr8:42896583-42897031 | Common:1; Rare:181 | ||||
| chr8:43056205-43056346 | Rare:50 | ||||
| chr8:43140297-43140588 | Common:3; Rare:112; Clinvar:10 |