| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28348779-28349178 | Common:3; Rare:127 | ||||
| chr3:29281011-29281081 | Rare:10 | ||||
| chr3:31532380-31532638 | Common:2; Rare:71 | ||||
| chr3:32106401-32106720 | Common:4; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32570636-32570920 | Rare:133 | ||||
| chr3:33277325-33277476 | Common:1; Rare:37 | ||||
| chr3:33798404-33798868 | Common:3; Rare:148 | ||||
| chr3:36993077-36993563 | Common:2; Rare:165; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37176315-37176397 | Rare:24 | ||||
| chr3:37243122-37243480 | Common:3; Rare:92 | ||||
| chr3:39051939-39052042 | Common:1; Rare:36 | ||||
| chr3:39107568-39107680 | Common:2; Rare:36 | ||||
| chr3:39153527-39153745 | Common:3; Rare:69 | ||||
| chr3:39406579-39406762 | Common:2; Rare:78 | ||||
| chr3:40309471-40309956 | Common:9; Rare:164 |