| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43955303-43955571 | Common:3; Rare:82 | ||||
| chr22:43998952-43999223 | Common:2; Rare:46 | ||||
| chr22:44024129-44024418 | Common:2; Rare:89 | ||||
| chr22:44086489-44086686 | Common:1; Rare:32 | ||||
| chr22:45163728-45164003 | Common:3; Rare:106 | ||||
| chr22:46053778-46054130 | Common:3; Rare:121 | ||||
| chr22:46250261-46250438 | Common:3; Rare:60 | ||||
| chr22:46335601-46335825 | Common:5; Rare:105; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762427-46762693 | Common:4; Rare:105 | ||||
| chr22:50185703-50185953 | Common:4; Rare:104 | ||||
| chr22:50244962-50245059 | Common:2; Rare:37 | ||||
| chr22:50582818-50583121 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50628079-50628261 | Common:8; Rare:89; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783611-50783853 | Common:2; Rare:73 | ||||
| chr3:3126908-3126990 | Common:1; Rare:34; Clinvar (benign):2 |