| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38030299-38030714 | Common:3; Rare:119 | ||||
| chr8:38105441-38105559 | Common:1; Rare:43 | ||||
| chr8:38105766-38105929 | Rare:50 | ||||
| chr8:38176430-38176875 | Common:5; Rare:126 | ||||
| chr8:38231692-38231781 | Rare:20 | ||||
| chr8:38269094-38269341 | Rare:92 | ||||
| chr8:38381810-38381883 | Rare:8 | ||||
| chr8:38386281-38386527 | Common:1; Rare:51 | ||||
| chr8:38404175-38404387 | Rare:62 | ||||
| chr8:38467991-38468168 | Rare:49; Clinvar (benign):2 | ||||
| chr8:38996443-38997107 | Common:7; Rare:254 | ||||
| chr8:40153292-40153502 | Common:2; Rare:47 | ||||
| chr8:42051954-42052266 | Common:1; Rare:87 | ||||
| chr8:42207533-42207727 | Common:2; Rare:58 | ||||
| chr8:42338390-42338509 | Common:1; Rare:49 |