| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25790008-25790126 | Common:4; Rare:45 | ||||
| chr3:28241439-28241673 | Common:1; Rare:79 | ||||
| chr3:28348612-28348865 | Common:1; Rare:72 | ||||
| chr3:28348868-28349196 | Common:3; Rare:106 | ||||
| chr3:29280837-29281617 | Common:16; Rare:152 | ||||
| chr3:30606291-30607025 | Common:2; Rare:213; Clinvar:9; Clinvar (benign):7 | ||||
| chr3:31532380-31532728 | Common:4; Rare:105 | ||||
| chr3:31533016-31533305 | Common:1; Rare:89; Clinvar (benign):2 | ||||
| chr3:31981603-31981811 | Common:1; Rare:54 | ||||
| chr3:32106425-32106744 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32238554-32238698 | Common:2; Rare:45 | ||||
| chr3:32502779-32502935 | Rare:43 | ||||
| chr3:32570645-32570956 | Common:1; Rare:139 | ||||
| chr3:32685051-32685445 | Rare:113 | ||||
| chr3:33096755-33096841 | Rare:28 |