| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:41577939-41578277 | Common:1; Rare:107 | ||||
| chr8:41578412-41578544 | Rare:37 | ||||
| chr8:41618689-41618978 | Rare:77 | ||||
| chr8:42051952-42052134 | Rare:48 | ||||
| chr8:42188909-42189141 | Rare:62 | ||||
| chr8:42207484-42207638 | Common:1; Rare:46 | ||||
| chr8:42207662-42207843 | Common:1; Rare:32 | ||||
| chr8:42271241-42271456 | Common:2; Rare:80 | ||||
| chr8:42319051-42319211 | Rare:20 | ||||
| chr8:42536287-42536357 | Rare:13 | ||||
| chr8:42541109-42541196 | Common:1; Rare:20 | ||||
| chr8:42541502-42541770 | Common:2; Rare:86 | ||||
| chr8:42541883-42542017 | Rare:32; Clinvar:3 | ||||
| chr8:42843046-42843153 | Rare:35; Clinvar:4; Clinvar (benign):1 | ||||
| chr8:42843213-42843267 | Rare:12; Clinvar:1 |