| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:33485022-33485224 | Common:2; Rare:70 | ||||
| chr8:37762453-37762678 | Common:2; Rare:81 | ||||
| chr8:37849838-37849952 | Common:1; Rare:49 | ||||
| chr8:38030278-38030611 | Common:3; Rare:98 | ||||
| chr8:38105356-38105569 | Common:3; Rare:67 | ||||
| chr8:38105677-38105938 | Common:1; Rare:86 | ||||
| chr8:38176398-38176551 | Common:1; Rare:58 | ||||
| chr8:38176650-38176906 | Common:5; Rare:71 | ||||
| chr8:38269104-38269288 | Rare:75 | ||||
| chr8:38467994-38468164 | Rare:48; Clinvar (benign):2 | ||||
| chr8:38901055-38901339 | Common:2; Rare:63 | ||||
| chr8:38901690-38901820 | Common:3; Rare:22 | ||||
| chr8:38996443-38997107 | Common:7; Rare:254 | ||||
| chr8:40153352-40153484 | Rare:30 | ||||
| chr8:41490358-41490636 | Rare:66 |