| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17628712-17628933 | Common:1; Rare:78 | ||||
| chr22:17638696-17638819 | Rare:43 | ||||
| chr22:18077826-18078032 | Common:4; Rare:70; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19291707-19291903 | Common:9; Rare:63 | ||||
| chr22:19432303-19432567 | Common:3; Rare:106 | ||||
| chr22:19447505-19447763 | Common:2; Rare:128 | ||||
| chr22:19479114-19479466 | Common:4; Rare:126 | ||||
| chr22:19854795-19854979 | Rare:63 | ||||
| chr22:19941729-19941877 | Rare:64; Clinvar:4; Clinvar (benign):4 | ||||
| chr22:20020897-20021143 | Common:1; Rare:81 | ||||
| chr22:20117175-20117571 | Common:3; Rare:127 | ||||
| chr22:20319991-20320133 | Common:2; Rare:51 | ||||
| chr22:20495775-20495925 | Common:2; Rare:56 | ||||
| chr22:20582938-20583152 | Rare:63 | ||||
| chr22:20858736-20859121 | Common:7; Rare:193; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 |