| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50343224-50343378 | Common:2; Rare:63 | ||||
| chr22:50525503-50525692 | Common:4; Rare:93; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:50562887-50563025 | Common:3; Rare:39 | ||||
| chr22:50582365-50582465 | Rare:45 | ||||
| chr22:50582769-50583171 | Common:9; Rare:147; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628082-50628286 | Common:9; Rare:100; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783597-50783822 | Common:2; Rare:74 | ||||
| chr3:3126813-3127105 | Common:5; Rare:115; Clinvar (benign):4 | ||||
| chr3:4303235-4303517 | Common:3; Rare:117 | ||||
| chr3:4493241-4493483 | Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:8501653-8501958 | Common:2; Rare:109 | ||||
| chr3:9249621-9249747 | Common:1; Rare:35 | ||||
| chr3:9362936-9363140 | Common:2; Rare:68 | ||||
| chr3:9397425-9397933 | Common:1; Rare:159 | ||||
| chr3:9749768-9750129 | Common:1; Rare:111 |