| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33645408-33645535 | Rare:15 | ||||
| chr3:33659062-33659455 | Common:3; Rare:68 | ||||
| chr3:33659580-33659755 | Rare:46 | ||||
| chr3:33798479-33798692 | Common:2; Rare:79 | ||||
| chr3:35638517-35638709 | Common:2; Rare:30 | ||||
| chr3:35638843-35638979 | Rare:27 | ||||
| chr3:35639423-35639579 | Common:3; Rare:38 | ||||
| chr3:35639581-35640106 | Common:3; Rare:114 | ||||
| chr3:35641572-35641654 | Common:2; Rare:13 | ||||
| chr3:35642143-35642401 | Rare:44 | ||||
| chr3:35643535-35643767 | Rare:54 | ||||
| chr3:35679457-35679650 | Rare:26 | ||||
| chr3:36993039-36993576 | Common:2; Rare:187; Clinvar:31; Clinvar (benign):14; Clinvar (pathogenic):3 | ||||
| chr3:37243166-37243348 | Common:1; Rare:48 | ||||
| chr3:37993875-37994160 | Common:1; Rare:81 |