| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25783383-25783621 | Common:2; Rare:79; Clinvar (benign):3 | ||||
| chr3:25790006-25790118 | Common:3; Rare:43 | ||||
| chr3:28348750-28348848 | Rare:37 | ||||
| chr3:28349007-28349178 | Common:2; Rare:49 | ||||
| chr3:29280852-29281081 | Common:3; Rare:43 | ||||
| chr3:30606324-30606521 | Common:1; Rare:46; Clinvar:1 | ||||
| chr3:31532380-31532664 | Common:4; Rare:83 | ||||
| chr3:31981627-31981820 | Common:1; Rare:50 | ||||
| chr3:32238554-32238706 | Common:2; Rare:47 | ||||
| chr3:32502779-32503028 | Rare:58 | ||||
| chr3:32570366-32570557 | Rare:60 | ||||
| chr3:32570623-32570919 | Rare:135 | ||||
| chr3:32684919-32685250 | Rare:90 | ||||
| chr3:33096722-33096836 | Rare:35 | ||||
| chr3:33114348-33114548 | Common:1; Rare:75; Clinvar:6; Clinvar (benign):4 |