| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141876486-141876682 | Common:1; Rare:74 | ||||
| chr3:143001448-143001631 | Common:2; Rare:66 | ||||
| chr3:143971711-143971829 | Common:1; Rare:54 | ||||
| chr3:146160962-146161386 | Common:2; Rare:128; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146163643-146163846 | Rare:32 | ||||
| chr3:146250974-146251274 | Common:2; Rare:74 | ||||
| chr3:146544514-146544869 | Common:4; Rare:85 | ||||
| chr3:148991392-148991632 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr3:149333204-149333703 | Common:4; Rare:118 | ||||
| chr3:149377369-149377821 | Common:1; Rare:136 | ||||
| chr3:149541040-149541192 | Common:1; Rare:33 | ||||
| chr3:149657943-149658170 | Rare:47 | ||||
| chr3:149812970-149813260 | Common:2; Rare:95 | ||||
| chr3:150408116-150408302 | Common:1; Rare:69 | ||||
| chr3:150603168-150603377 | Common:2; Rare:84 |