| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:11154375-11154535 | Common:3; Rare:43 | ||||
| chr3:11719419-11719566 | Rare:48 | ||||
| chr3:12484333-12484554 | Common:5; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12663974-12664300 | Common:2; Rare:91; Clinvar:2; Clinvar (benign):7 | ||||
| chr3:12796590-12796707 | Common:3; Rare:40 | ||||
| chr3:13420231-13420466 | Common:1; Rare:69 | ||||
| chr3:13480040-13480339 | Common:2; Rare:70 | ||||
| chr3:14124697-14125186 | Common:4; Rare:143; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178466-14178876 | Common:3; Rare:197; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14402437-14402722 | Rare:65 | ||||
| chr3:14651463-14651818 | Rare:105 | ||||
| chr3:14947208-14947559 | Common:4; Rare:156 | ||||
| chr3:14948024-14948340 | Rare:140 | ||||
| chr3:14948363-14948641 | Common:2; Rare:78 | ||||
| chr3:15205982-15206294 | Common:1; Rare:117 |