| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69332713-69332874 | Rare:68 | ||||
| chr5:69369450-69369913 | Common:3; Rare:358 | ||||
| chr5:69369930-69370230 | Common:2; Rare:111 | ||||
| chr5:69492664-69492830 | Rare:96; Clinvar (benign):1 | ||||
| chr5:69559942-69560290 | Common:6; Rare:143 | ||||
| chr5:71586587-71586877 | Common:4; Rare:110 | ||||
| chr5:71587132-71587420 | Common:2; Rare:192; Clinvar (benign):4 | ||||
| chr5:72107123-72107512 | Common:2; Rare:149 | ||||
| chr5:72308263-72308595 | Common:4; Rare:193 | ||||
| chr5:72319896-72320663 | Rare:609 | ||||
| chr5:72955860-72956094 | Common:2; Rare:198 | ||||
| chr5:73498305-73498570 | Common:6; Rare:162 | ||||
| chr5:73565286-73565858 | Common:13; Rare:294 | ||||
| chr5:73625963-73626291 | Common:6; Rare:159 | ||||
| chr5:73813217-73813598 | Common:2; Rare:151 |