| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:60700129-60700233 | Common:1; Rare:30 | ||||
| chr5:60945038-60945253 | Common:4; Rare:79; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:61162350-61162481 | Rare:23 | ||||
| chr5:62403789-62404044 | Common:3; Rare:95 | ||||
| chr5:64768418-64768454 | Common:1; Rare:10 | ||||
| chr5:64768509-64769031 | Common:5; Rare:140 | ||||
| chr5:65481836-65482034 | Common:1; Rare:37 | ||||
| chr5:65563124-65563406 | Common:3; Rare:113 | ||||
| chr5:65624981-65625074 | Rare:33 | ||||
| chr5:65722059-65722384 | Common:4; Rare:109 | ||||
| chr5:65925582-65925980 | Rare:152 | ||||
| chr5:66144154-66144351 | Common:2; Rare:69 | ||||
| chr5:67004062-67004289 | Common:3; Rare:81 | ||||
| chr5:67196728-67197017 | Common:3; Rare:54 | ||||
| chr5:68215458-68215828 | Common:4; Rare:125 |