| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:71587186-71587413 | Common:1; Rare:72; Clinvar (benign):2 | ||||
| chr5:72179410-72179826 | Common:1; Rare:82 | ||||
| chr5:72179855-72179993 | Common:1; Rare:15 | ||||
| chr5:72507374-72507630 | Common:1; Rare:39 | ||||
| chr5:72816496-72816706 | Common:3; Rare:77 | ||||
| chr5:72848070-72848183 | Common:3; Rare:46 | ||||
| chr5:72955849-72956085 | Common:1; Rare:110 | ||||
| chr5:73498315-73498572 | Common:3; Rare:78 | ||||
| chr5:73565369-73565831 | Common:7; Rare:143 | ||||
| chr5:74640719-74640856 | Common:1; Rare:36 | ||||
| chr5:74720338-74720505 | Rare:46; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:74767059-74767347 | Common:2; Rare:90 | ||||
| chr5:75336901-75337242 | Common:2; Rare:114 | ||||
| chr5:75511606-75511941 | Common:1; Rare:120 | ||||
| chr5:78294661-78294825 | Rare:67; Clinvar:1 |