| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50504908-50505254 | Common:2; Rare:179 | ||||
| chr22:50506466-50506629 | Common:1; Rare:70 | ||||
| chr22:50525547-50525661 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50562887-50563044 | Common:3; Rare:45 | ||||
| chr22:50582818-50583142 | Common:5; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50628087-50628276 | Common:9; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783623-50783846 | Common:1; Rare:68 | ||||
| chr3:3126783-3127016 | Common:4; Rare:103; Clinvar (benign):4 | ||||
| chr3:4303247-4303412 | Common:2; Rare:66 | ||||
| chr3:4493177-4493483 | Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4979145-4979530 | Common:2; Rare:89 | ||||
| chr3:5187287-5187663 | Common:5; Rare:140 | ||||
| chr3:8501616-8501937 | Common:2; Rare:120 | ||||
| chr3:9249627-9249743 | Common:1; Rare:34 | ||||
| chr3:9362966-9363098 | Common:1; Rare:48 |