| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42070802-42070983 | Common:3; Rare:39 | ||||
| chr22:42079629-42079763 | Common:1; Rare:40 | ||||
| chr22:42090740-42090953 | Common:1; Rare:72; Clinvar (pathogenic):1 | ||||
| chr22:42614863-42615244 | Common:3; Rare:153 | ||||
| chr22:45163765-45164008 | Common:2; Rare:94 | ||||
| chr22:46053777-46053856 | Rare:28 | ||||
| chr22:46250276-46250430 | Common:2; Rare:53 | ||||
| chr22:46335595-46335760 | Common:2; Rare:71; Clinvar:7; Clinvar (benign):6 | ||||
| chr22:46762506-46762663 | Common:3; Rare:55 | ||||
| chr22:50244973-50245114 | Common:1; Rare:57 | ||||
| chr22:50628150-50628263 | Common:6; Rare:58 | ||||
| chr22:50783616-50783835 | Common:2; Rare:67 | ||||
| chr3:196982-197296 | Common:3; Rare:116 | ||||
| chr3:2098616-2098962 | Common:4; Rare:137 | ||||
| chr3:4493181-4493348 | Rare:60 |