| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:31532380-31532683 | Common:4; Rare:89 | ||||
| chr3:31533051-31533305 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr3:32106376-32106720 | Common:4; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32238584-32238897 | Common:2; Rare:76 | ||||
| chr3:32502749-32502938 | Rare:57 | ||||
| chr3:32570635-32570950 | Common:1; Rare:143 | ||||
| chr3:33097062-33097233 | Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:33114420-33114530 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:33277312-33277495 | Common:1; Rare:50 | ||||
| chr3:33718061-33718295 | Rare:85 | ||||
| chr3:33798499-33798895 | Common:3; Rare:138 | ||||
| chr3:33798985-33799154 | Rare:52 | ||||
| chr3:36993039-36993580 | Common:2; Rare:189; Clinvar:32; Clinvar (benign):15; Clinvar (pathogenic):3 | ||||
| chr3:36993663-36993826 | Rare:67; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:37176290-37176393 | Rare:32 |