| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:71725210-71725527 | Common:2; Rare:113 | ||||
| chr3:71729028-71729239 | Rare:35 | ||||
| chr3:71753560-71753748 | Common:3; Rare:82 | ||||
| chr3:71754722-71754953 | Rare:60 | ||||
| chr3:71755050-71755417 | Rare:90 | ||||
| chr3:72996666-72997047 | Common:2; Rare:148 | ||||
| chr3:77039318-77039432 | Rare:20 | ||||
| chr3:77039731-77040167 | Common:3; Rare:133 | ||||
| chr3:77040215-77040483 | Common:3; Rare:53; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:77040607-77040843 | Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:79018489-79018552 | Rare:13 | ||||
| chr3:79018715-79019079 | Common:1; Rare:99 | ||||
| chr3:79019343-79019554 | Common:3; Rare:67 | ||||
| chr3:79767712-79768178 | Common:4; Rare:75 | ||||
| chr3:79768181-79768307 | Common:2; Rare:25 |