| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:30095288-30095507 | Common:2; Rare:68 | ||||
| chr8:30156243-30156405 | Rare:49 | ||||
| chr8:30658127-30658397 | Common:5; Rare:89 | ||||
| chr8:33485009-33485228 | Common:2; Rare:77 | ||||
| chr8:37762452-37762678 | Common:2; Rare:82 | ||||
| chr8:37849824-37850002 | Common:1; Rare:65 | ||||
| chr8:38030283-38030708 | Common:3; Rare:121 | ||||
| chr8:38105356-38105553 | Common:2; Rare:60 | ||||
| chr8:38105778-38105945 | Rare:49 | ||||
| chr8:38176406-38176883 | Common:5; Rare:142 | ||||
| chr8:38996272-38996293 | Rare:12 | ||||
| chr8:38996421-38997145 | Common:8; Rare:271; Clinvar (benign):1 | ||||
| chr8:40153386-40153541 | Common:1; Rare:37 | ||||
| chr8:42051976-42052254 | Common:1; Rare:80 | ||||
| chr8:42540925-42541179 | Rare:65 |