| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69217621-69217921 | Common:4; Rare:103 | ||||
| chr5:69234769-69234953 | Common:1; Rare:52 | ||||
| chr5:69332739-69332870 | Rare:34 | ||||
| chr5:69369371-69369922 | Common:2; Rare:220 | ||||
| chr5:69369965-69370067 | Common:1; Rare:23 | ||||
| chr5:69560088-69560290 | Common:3; Rare:50 | ||||
| chr5:71455519-71456036 | Common:1; Rare:173; Clinvar (benign):1 | ||||
| chr5:72107024-72107715 | Common:3; Rare:229 | ||||
| chr5:72816496-72816718 | Common:4; Rare:82 | ||||
| chr5:72955869-72956105 | Common:1; Rare:102 | ||||
| chr5:73498298-73498660 | Common:3; Rare:117 | ||||
| chr5:73498780-73498790 | Rare:2 | ||||
| chr5:73565370-73565848 | Common:7; Rare:151 | ||||
| chr5:74640474-74640958 | Common:3; Rare:148 | ||||
| chr5:74767019-74767482 | Common:5; Rare:131 |