| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:5187376-5187742 | Common:6; Rare:153 | ||||
| chr3:8501638-8501956 | Common:2; Rare:116 | ||||
| chr3:9362972-9363130 | Common:1; Rare:56 | ||||
| chr3:9397437-9397935 | Common:1; Rare:152 | ||||
| chr3:9749772-9750137 | Common:1; Rare:110 | ||||
| chr3:9792300-9792611 | Common:1; Rare:83 | ||||
| chr3:9792623-9793127 | Common:4; Rare:171 | ||||
| chr3:9933514-9933868 | Common:2; Rare:145; Clinvar:3 | ||||
| chr3:10026304-10026486 | Rare:57 | ||||
| chr3:10306097-10306395 | Common:4; Rare:54 | ||||
| chr3:11154392-11154538 | Common:3; Rare:39 | ||||
| chr3:12556759-12557161 | Common:5; Rare:112 | ||||
| chr3:12663816-12664229 | Common:2; Rare:116; Clinvar:6; Clinvar (benign):10 | ||||
| chr3:14124719-14125179 | Common:4; Rare:134; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178513-14178866 | Common:3; Rare:180; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 |