| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:72955839-72956112 | Common:1; Rare:117 | ||||
| chr5:73498330-73498669 | Common:3; Rare:104 | ||||
| chr5:73565360-73565826 | Common:7; Rare:144 | ||||
| chr5:74640510-74640659 | Common:1; Rare:39 | ||||
| chr5:74685119-74685422 | Common:2; Rare:113; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr5:74685478-74685556 | Rare:17 | ||||
| chr5:74720429-74720716 | Common:1; Rare:85; Clinvar:2; Clinvar (pathogenic):4 | ||||
| chr5:74733076-74733214 | Rare:22; Clinvar:1 | ||||
| chr5:74767007-74767362 | Common:3; Rare:109 | ||||
| chr5:75336907-75337290 | Common:3; Rare:133 | ||||
| chr5:75511610-75511913 | Common:1; Rare:112 | ||||
| chr5:75717345-75717670 | Common:5; Rare:85 | ||||
| chr5:76623316-76623619 | Common:2; Rare:61 | ||||
| chr5:77087192-77087355 | Rare:34 | ||||
| chr5:78360365-78360726 | Common:5; Rare:136 |