| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:22412200-22412504 | Common:1; Rare:66 | ||||
| chr8:22440949-22441295 | Common:7; Rare:90 | ||||
| chr8:22589179-22589349 | Common:1; Rare:66 | ||||
| chr8:22604534-22604820 | Common:1; Rare:106 | ||||
| chr8:22669088-22669169 | Common:2; Rare:30 | ||||
| chr8:23068957-23069219 | Common:1; Rare:109 | ||||
| chr8:23164010-23164118 | Rare:20 | ||||
| chr8:23224979-23225248 | Common:1; Rare:74 | ||||
| chr8:23225381-23225522 | Common:3; Rare:21; Clinvar:1 | ||||
| chr8:23457617-23457848 | Common:3; Rare:82 | ||||
| chr8:23528623-23529111 | Rare:151 | ||||
| chr8:23541506-23541762 | Common:3; Rare:50 | ||||
| chr8:24955942-24956192 | Rare:92; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr8:24956544-24956671 | Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:25458202-25458638 | Common:2; Rare:123 |