| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:91040818-91040985 | Common:2; Rare:51 | ||||
| chr8:91070002-91070425 | Common:1; Rare:153 | ||||
| chr8:93700310-93700616 | Common:1; Rare:100 | ||||
| chr8:93740944-93741191 | Common:1; Rare:81 | ||||
| chr8:93754768-93754938 | Common:1; Rare:60; Clinvar (benign):4 | ||||
| chr8:93916628-93916940 | Common:4; Rare:98; Clinvar (benign):1 | ||||
| chr8:94262313-94262433 | Rare:33 | ||||
| chr8:94475047-94475188 | Common:3; Rare:39 | ||||
| chr8:94553445-94553763 | Common:3; Rare:112 | ||||
| chr8:94719765-94719941 | Common:1; Rare:50 | ||||
| chr8:94822959-94823260 | Common:1; Rare:89 | ||||
| chr8:94895194-94895345 | Rare:49 | ||||
| chr8:94895679-94895822 | Common:1; Rare:44 | ||||
| chr8:94949364-94949487 | Common:1; Rare:40 | ||||
| chr8:95024754-95025120 | Common:2; Rare:127; Clinvar:1; Clinvar (benign):8; Clinvar (pathogenic):1 |