| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:1092777-1093169 | Common:1; Rare:107 | ||||
| chr3:2098556-2098978 | Common:4; Rare:165 | ||||
| chr3:3126813-3127026 | Common:4; Rare:96; Clinvar (benign):4 | ||||
| chr3:3799789-3799917 | Common:1; Rare:43 | ||||
| chr3:4303253-4303412 | Common:1; Rare:62 | ||||
| chr3:4467246-4467291 | Rare:23; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493177-4493350 | Rare:61 | ||||
| chr3:4979142-4979539 | Common:2; Rare:93 | ||||
| chr3:5122432-5122515 | Common:1; Rare:26 | ||||
| chr3:5187320-5187590 | Common:4; Rare:107 | ||||
| chr3:6862615-6862791 | Common:3; Rare:60 | ||||
| chr3:8501620-8501858 | Rare:86 | ||||
| chr3:9249543-9249758 | Common:2; Rare:44 | ||||
| chr3:9362936-9363117 | Common:2; Rare:65 | ||||
| chr3:9397418-9397692 | Common:1; Rare:103 |