| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9843952-9844128 | Common:2; Rare:74 | ||||
| chr3:9890474-9890696 | Common:2; Rare:90 | ||||
| chr3:9916897-9917317 | Common:5; Rare:97 | ||||
| chr3:9933507-9933896 | Common:3; Rare:155; Clinvar:3 | ||||
| chr3:9986766-9987169 | Common:4; Rare:115 | ||||
| chr3:10026304-10026473 | Rare:54 | ||||
| chr3:10115524-10115779 | Common:3; Rare:88 | ||||
| chr3:10141680-10142000 | Common:1; Rare:154; Clinvar:39; Clinvar (benign):33 | ||||
| chr3:11154337-11154542 | Common:4; Rare:54 | ||||
| chr3:11719419-11719595 | Rare:57 | ||||
| chr3:12158717-12158990 | Rare:118 | ||||
| chr3:12159357-12159464 | Common:1; Rare:17 | ||||
| chr3:12288834-12289068 | Common:1; Rare:47 | ||||
| chr3:12484321-12484570 | Common:5; Rare:82; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12664073-12664330 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):3 |