| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:40153154-40153484 | Common:3; Rare:61 | ||||
| chr8:41490355-41490664 | Common:1; Rare:78 | ||||
| chr8:41577985-41578262 | Rare:88 | ||||
| chr8:41578364-41578528 | Rare:46 | ||||
| chr8:42051954-42052272 | Common:1; Rare:89 | ||||
| chr8:42391772-42391925 | Common:1; Rare:52 | ||||
| chr8:42541131-42541182 | Rare:10 | ||||
| chr8:42541489-42541765 | Common:2; Rare:86 | ||||
| chr8:42541923-42542062 | Rare:40; Clinvar:3 | ||||
| chr8:42842789-42843004 | Common:2; Rare:69 | ||||
| chr8:42843030-42843096 | Rare:17; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr8:42843098-42843137 | Rare:19; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:42843170-42843485 | Common:2; Rare:81; Clinvar:2; Clinvar (benign):3 | ||||
| chr8:42896546-42897037 | Common:1; Rare:197 | ||||
| chr8:42897254-42897394 | Common:1; Rare:38 |