| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46762496-46762701 | Common:3; Rare:76 | ||||
| chr22:49918372-49918684 | Common:2; Rare:114; Clinvar (benign):1 | ||||
| chr22:50185703-50185953 | Common:4; Rare:104 | ||||
| chr22:50190410-50190610 | Common:2; Rare:62 | ||||
| chr22:50244954-50245086 | Common:2; Rare:51 | ||||
| chr22:50525523-50525697 | Common:4; Rare:84; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50532117-50532409 | Common:2; Rare:66 | ||||
| chr22:50562886-50563065 | Common:3; Rare:48 | ||||
| chr22:50582818-50583120 | Common:5; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50627975-50628288 | Common:9; Rare:125; Clinvar:4; Clinvar (benign):1 | ||||
| chr22:50783592-50783842 | Common:2; Rare:84 | ||||
| chr3:197257-197338 | Rare:25 | ||||
| chr3:2098603-2098970 | Common:4; Rare:148 | ||||
| chr3:3126773-3127017 | Common:4; Rare:111; Clinvar (benign):4 | ||||
| chr3:4303222-4303651 | Common:4; Rare:162 |