| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141876491-141876652 | Common:1; Rare:60 | ||||
| chr3:142447974-142448163 | Common:1; Rare:73 | ||||
| chr3:142578710-142578980 | Rare:100; Clinvar:1 | ||||
| chr3:142888883-142889228 | Common:3; Rare:73 | ||||
| chr3:143001199-143001650 | Common:5; Rare:123 | ||||
| chr3:143971754-143971847 | Common:1; Rare:43 | ||||
| chr3:146160910-146161387 | Common:2; Rare:150; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146163660-146163857 | Rare:31 | ||||
| chr3:146544540-146544890 | Common:4; Rare:82 | ||||
| chr3:148991390-148991620 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr3:149129545-149129711 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377380-149377818 | Common:1; Rare:134 | ||||
| chr3:149812602-149812747 | Common:1; Rare:38 | ||||
| chr3:149813004-149813269 | Common:2; Rare:87 | ||||
| chr3:149969224-149969460 | Common:2; Rare:65 |