| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38030383-38030595 | Common:2; Rare:65 | ||||
| chr8:38105350-38105569 | Common:3; Rare:69 | ||||
| chr8:38105779-38106006 | Rare:70 | ||||
| chr8:38176449-38176571 | Common:1; Rare:42 | ||||
| chr8:38176682-38176890 | Common:3; Rare:62 | ||||
| chr8:38267301-38267611 | Common:1; Rare:85 | ||||
| chr8:38381841-38381876 | Rare:3 | ||||
| chr8:38996447-38997012 | Common:7; Rare:209 | ||||
| chr8:41578007-41578256 | Rare:80 | ||||
| chr8:42391783-42391920 | Common:1; Rare:47 | ||||
| chr8:42541044-42541182 | Rare:35 | ||||
| chr8:42541494-42541687 | Common:2; Rare:58 | ||||
| chr8:42541691-42542014 | Common:1; Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:42843045-42843099 | Rare:11; Clinvar:2 | ||||
| chr8:42896587-42897027 | Common:1; Rare:179 |