| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:27722708-27722944 | Common:3; Rare:32 | ||||
| chr3:28241558-28241768 | Common:2; Rare:73 | ||||
| chr3:28291732-28291849 | Common:1; Rare:24 | ||||
| chr3:28348607-28349196 | Common:4; Rare:178 | ||||
| chr3:29280829-29281456 | Common:15; Rare:124 | ||||
| chr3:30606259-30606521 | Common:1; Rare:60; Clinvar:1 | ||||
| chr3:32106378-32106697 | Common:4; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502779-32502915 | Rare:41 | ||||
| chr3:32570668-32570970 | Common:1; Rare:128 | ||||
| chr3:32685085-32685386 | Rare:87 | ||||
| chr3:33097097-33097265 | Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277289-33277498 | Common:2; Rare:58 | ||||
| chr3:33645448-33645559 | Rare:12 | ||||
| chr3:33658997-33659455 | Common:3; Rare:85 | ||||
| chr3:33659505-33659739 | Rare:56 |