| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:41578375-41578480 | Rare:29 | ||||
| chr8:41797606-41797803 | Common:2; Rare:53; Clinvar (pathogenic):2 | ||||
| chr8:42051962-42052266 | Common:1; Rare:86 | ||||
| chr8:42152733-42153098 | Common:3; Rare:94 | ||||
| chr8:42271251-42271354 | Rare:34 | ||||
| chr8:42338354-42338525 | Common:1; Rare:72 | ||||
| chr8:42391529-42391926 | Common:4; Rare:120 | ||||
| chr8:42501048-42501487 | Common:1; Rare:85 | ||||
| chr8:42541104-42541415 | Common:1; Rare:72 | ||||
| chr8:42541476-42541893 | Common:3; Rare:130; Clinvar (benign):1 | ||||
| chr8:42541895-42542013 | Rare:28; Clinvar:2 | ||||
| chr8:42542021-42542082 | Rare:16 | ||||
| chr8:42542135-42542208 | Rare:21; Clinvar (benign):1 | ||||
| chr8:42842860-42842996 | Common:1; Rare:44 | ||||
| chr8:42843039-42843100 | Rare:13; Clinvar:2 |