| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:62361244-62361527 | Common:1; Rare:44; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr5:62403802-62404052 | Common:3; Rare:91 | ||||
| chr5:62412543-62412907 | Common:1; Rare:119 | ||||
| chr5:64768524-64769006 | Common:5; Rare:128 | ||||
| chr5:65554811-65555161 | Common:3; Rare:85 | ||||
| chr5:65563081-65563421 | Common:4; Rare:133 | ||||
| chr5:65624649-65624825 | Common:8; Rare:24 | ||||
| chr5:65624959-65625054 | Common:1; Rare:33 | ||||
| chr5:65721959-65722296 | Common:2; Rare:106 | ||||
| chr5:65925564-65926020 | Rare:167 | ||||
| chr5:65926440-65926791 | Common:5; Rare:99 | ||||
| chr5:66144480-66144535 | Rare:17 | ||||
| chr5:67004089-67004162 | Rare:32 | ||||
| chr5:69166890-69167281 | Common:3; Rare:104 | ||||
| chr5:69189440-69189753 | Common:1; Rare:103 |