| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38787881-38788172 | Common:2; Rare:59 | ||||
| chr8:38805236-38805477 | Common:1; Rare:37 | ||||
| chr8:38901104-38901339 | Common:1; Rare:52 | ||||
| chr8:38901341-38901362 | Rare:7 | ||||
| chr8:38901714-38901851 | Common:2; Rare:25 | ||||
| chr8:38996455-38997051 | Common:7; Rare:224 | ||||
| chr8:40153341-40153546 | Common:1; Rare:53 | ||||
| chr8:41490223-41490475 | Rare:58 | ||||
| chr8:42051964-42052263 | Common:1; Rare:85 | ||||
| chr8:42338395-42338509 | Common:1; Rare:48 | ||||
| chr8:42391797-42391925 | Common:1; Rare:42 | ||||
| chr8:42540958-42541178 | Rare:58 | ||||
| chr8:42541484-42541765 | Common:2; Rare:86 | ||||
| chr8:42541895-42542002 | Rare:25; Clinvar:2 | ||||
| chr8:42542135-42542150 | Rare:7; Clinvar (benign):1 |