| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38105755-38105931 | Rare:55 | ||||
| chr8:38176430-38176890 | Common:6; Rare:133 | ||||
| chr8:38269123-38269234 | Rare:46 | ||||
| chr8:38382148-38382411 | Common:2; Rare:80 | ||||
| chr8:38466171-38466313 | Common:2; Rare:45 | ||||
| chr8:38467692-38468097 | Common:3; Rare:134; Clinvar (benign):1 | ||||
| chr8:38786988-38787234 | Rare:91 | ||||
| chr8:38901082-38901444 | Common:3; Rare:87 | ||||
| chr8:38901690-38901871 | Common:3; Rare:31 | ||||
| chr8:38996447-38997066 | Common:7; Rare:234 | ||||
| chr8:40153341-40153613 | Common:2; Rare:79 | ||||
| chr8:42051954-42052263 | Common:1; Rare:87 | ||||
| chr8:42207645-42207928 | Common:2; Rare:54 | ||||
| chr8:42271243-42271485 | Common:2; Rare:91 | ||||
| chr8:42541026-42541189 | Common:1; Rare:44 |