| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38105766-38105966 | Rare:58 | ||||
| chr8:38176436-38176530 | Common:1; Rare:34 | ||||
| chr8:38176674-38176863 | Common:4; Rare:51 | ||||
| chr8:38269167-38269269 | Rare:39 | ||||
| chr8:38727948-38728213 | Common:2; Rare:51 | ||||
| chr8:38901021-38901352 | Common:2; Rare:76 | ||||
| chr8:38901701-38901836 | Common:3; Rare:22 | ||||
| chr8:38996455-38997051 | Common:7; Rare:224 | ||||
| chr8:41665184-41665258 | Common:1; Rare:21 | ||||
| chr8:41665267-41665290 | Rare:5 | ||||
| chr8:41665378-41665427 | Rare:4 | ||||
| chr8:41665774-41665857 | Common:1; Rare:11 | ||||
| chr8:42540921-42541178 | Rare:66 | ||||
| chr8:42541489-42541872 | Common:3; Rare:126; Clinvar (benign):1 | ||||
| chr8:42541875-42541940 | Rare:14 |