| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:41490355-41490613 | Rare:60 | ||||
| chr8:41528958-41529261 | Common:3; Rare:63 | ||||
| chr8:41577932-41578249 | Rare:99 | ||||
| chr8:41665257-41665326 | Common:1; Rare:12 | ||||
| chr8:42051976-42052272 | Common:1; Rare:86 | ||||
| chr8:42338390-42338509 | Common:1; Rare:49 | ||||
| chr8:42391757-42391920 | Common:1; Rare:55 | ||||
| chr8:42541561-42541666 | Rare:36 | ||||
| chr8:42541691-42541932 | Common:1; Rare:79; Clinvar (benign):1 | ||||
| chr8:42843046-42843092 | Rare:11; Clinvar:2 | ||||
| chr8:42843283-42843516 | Common:2; Rare:67; Clinvar (benign):3 | ||||
| chr8:42896683-42897027 | Common:1; Rare:140 | ||||
| chr8:43056153-43056452 | Common:1; Rare:117 | ||||
| chr8:43093416-43093550 | Common:2; Rare:26 | ||||
| chr8:47260781-47260981 | Common:3; Rare:87 |