| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38030213-38030654 | Common:4; Rare:123 | ||||
| chr8:38105352-38105550 | Common:2; Rare:59 | ||||
| chr8:38105758-38105975 | Rare:64 | ||||
| chr8:38176406-38176870 | Common:5; Rare:138 | ||||
| chr8:38996443-38997045 | Common:7; Rare:229 | ||||
| chr8:42541494-42541764 | Common:2; Rare:85 | ||||
| chr8:42542141-42542184 | Rare:11; Clinvar (benign):1 | ||||
| chr8:42896289-42897031 | Common:3; Rare:324 | ||||
| chr8:43093440-43093555 | Common:3; Rare:25; Clinvar (benign):1 | ||||
| chr8:47260787-47260989 | Common:3; Rare:89 | ||||
| chr8:48008376-48008460 | Common:1; Rare:52 | ||||
| chr8:48921376-48921709 | Common:1; Rare:73 | ||||
| chr8:51899055-51899317 | Common:4; Rare:118 | ||||
| chr8:52714394-52714545 | Common:1; Rare:62 | ||||
| chr8:54135117-54135286 | Common:3; Rare:58 |