| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46150307-46150646 | Common:1; Rare:109 | ||||
| chr22:46151755-46151917 | Common:1; Rare:29 | ||||
| chr22:46250268-46250408 | Common:1; Rare:45 | ||||
| chr22:46267808-46268072 | Common:1; Rare:83 | ||||
| chr22:46335404-46335792 | Common:7; Rare:137; Clinvar:12; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762476-46762701 | Common:3; Rare:85 | ||||
| chr22:49918408-49918710 | Common:1; Rare:113 | ||||
| chr22:50185725-50185953 | Common:4; Rare:95 | ||||
| chr22:50244954-50245078 | Common:2; Rare:48 | ||||
| chr22:50443524-50443540 | Rare:3 | ||||
| chr22:50447392-50447636 | Common:1; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50525521-50525685 | Common:4; Rare:80; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50562887-50563059 | Common:3; Rare:46 | ||||
| chr22:50582777-50583142 | Common:7; Rare:124; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50627981-50628278 | Common:9; Rare:120; Clinvar:4; Clinvar (benign):1 |