| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:16264860-16265243 | Common:2; Rare:132 | ||||
| chr3:16513623-16513871 | Common:4; Rare:65 | ||||
| chr3:17742591-17742952 | Common:4; Rare:127 | ||||
| chr3:19946974-19947450 | Common:7; Rare:177 | ||||
| chr3:20186176-20186415 | Common:2; Rare:77 | ||||
| chr3:23202950-23203198 | Rare:84 | ||||
| chr3:23916855-23917238 | Rare:141 | ||||
| chr3:25428106-25428378 | Rare:60 | ||||
| chr3:25783392-25783634 | Common:2; Rare:77; Clinvar (benign):3 | ||||
| chr3:28348618-28348727 | Rare:24 | ||||
| chr3:28348779-28349231 | Common:4; Rare:143 | ||||
| chr3:29280831-29281428 | Common:15; Rare:114 | ||||
| chr3:30606341-30606514 | Rare:43; Clinvar:1 | ||||
| chr3:31981625-31981780 | Rare:44 | ||||
| chr3:32106418-32106636 | Common:4; Rare:56; Clinvar:2; Clinvar (benign):1 |