| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123396355-123396562 | Common:4; Rare:185 | ||||
| chr8:123396600-123396853 | Common:1; Rare:82 | ||||
| chr8:123416294-123416842 | Common:2; Rare:285 | ||||
| chr8:123416926-123417055 | Rare:42 | ||||
| chr8:123768289-123768623 | Common:9; Rare:184 | ||||
| chr8:124372644-124372839 | Common:3; Rare:148 | ||||
| chr8:124474150-124474440 | Common:2; Rare:97 | ||||
| chr8:124474509-124474939 | Common:3; Rare:286 | ||||
| chr8:124474946-124475102 | Rare:86 | ||||
| chr8:124538981-124539278 | Common:4; Rare:274; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr8:124542946-124543247 | Common:3; Rare:80; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:124726831-124727380 | Rare:189 | ||||
| chr8:124727464-124727930 | Common:3; Rare:207 | ||||
| chr8:124728388-124728624 | Rare:131 | ||||
| chr8:124998139-124998969 | Common:20; Rare:555 |