| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38105720-38105935 | Rare:69 | ||||
| chr8:38176409-38176564 | Common:1; Rare:61 | ||||
| chr8:38176657-38176872 | Common:4; Rare:57 | ||||
| chr8:38901095-38901352 | Common:1; Rare:58 | ||||
| chr8:38996263-38996299 | Common:1; Rare:22 | ||||
| chr8:38996447-38997156 | Common:8; Rare:267; Clinvar (benign):1 | ||||
| chr8:42541114-42541182 | Rare:14 | ||||
| chr8:42541494-42541779 | Common:2; Rare:92 | ||||
| chr8:42542135-42542356 | Common:2; Rare:50; Clinvar (benign):1 | ||||
| chr8:42843081-42843108 | Rare:6 | ||||
| chr8:42896262-42896397 | Rare:57 | ||||
| chr8:42896509-42897173 | Common:1; Rare:250 | ||||
| chr8:42897266-42897331 | Rare:15 | ||||
| chr8:47260730-47260989 | Common:3; Rare:115 | ||||
| chr8:47960112-47960267 | Common:1; Rare:53; Clinvar (benign):1 |