| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42013426-42013830 | Common:7; Rare:117 | ||||
| chr3:42502425-42502643 | Common:1; Rare:50 | ||||
| chr3:42581680-42581730 | Rare:13 | ||||
| chr3:42581867-42582185 | Common:3; Rare:100 | ||||
| chr3:42582289-42582461 | Common:2; Rare:42 | ||||
| chr3:42590503-42591024 | Common:5; Rare:151 | ||||
| chr3:42600262-42600889 | Common:3; Rare:223 | ||||
| chr3:42600941-42601309 | Common:1; Rare:126 | ||||
| chr3:42654148-42654633 | Common:2; Rare:125 | ||||
| chr3:42772710-42772841 | Common:1; Rare:34 | ||||
| chr3:42773069-42773393 | Common:3; Rare:87 | ||||
| chr3:42804386-42804772 | Common:4; Rare:115 | ||||
| chr3:43286449-43286630 | Common:2; Rare:82 | ||||
| chr3:43621835-43622391 | Common:2; Rare:163; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43638927-43639174 | Common:2; Rare:44 |