| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:68292024-68292333 | Common:3; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:69166927-69167248 | Common:2; Rare:84 | ||||
| chr5:69332718-69332855 | Rare:35 | ||||
| chr5:69369466-69369877 | Common:1; Rare:169 | ||||
| chr5:69492671-69492840 | Rare:54; Clinvar (benign):1 | ||||
| chr5:71587194-71587413 | Common:1; Rare:68; Clinvar (benign):2 | ||||
| chr5:72816487-72816740 | Common:4; Rare:94 | ||||
| chr5:72955754-72956080 | Common:1; Rare:137 | ||||
| chr5:73120474-73120689 | Common:2; Rare:52 | ||||
| chr5:73498305-73498652 | Common:3; Rare:110 | ||||
| chr5:73565420-73565775 | Common:6; Rare:101 | ||||
| chr5:74640448-74640667 | Common:1; Rare:59 | ||||
| chr5:74640719-74640859 | Common:1; Rare:37 | ||||
| chr5:74718587-74718952 | Common:1; Rare:94; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr5:74767043-74767308 | Common:2; Rare:78 |