| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42614853-42615251 | Common:3; Rare:166 | ||||
| chr22:42649323-42649482 | Common:1; Rare:63 | ||||
| chr22:43089313-43089496 | Common:3; Rare:62 | ||||
| chr22:43955303-43955571 | Common:3; Rare:82 | ||||
| chr22:45163694-45164008 | Common:4; Rare:113 | ||||
| chr22:46250257-46250396 | Common:2; Rare:39 | ||||
| chr22:46267870-46268032 | Common:1; Rare:49 | ||||
| chr22:46296676-46296919 | Common:2; Rare:88 | ||||
| chr22:46335621-46335801 | Common:5; Rare:82; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762503-46762661 | Common:3; Rare:56 | ||||
| chr22:50582818-50583161 | Common:6; Rare:112; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50628139-50628263 | Common:6; Rare:62; Clinvar:1 | ||||
| chr22:50783628-50783859 | Common:1; Rare:66 | ||||
| chr3:8501644-8501899 | Common:1; Rare:91 | ||||
| chr3:9362971-9363098 | Common:1; Rare:46 |