| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:13451758-13452089 | Common:11; Rare:205 | ||||
| chr3:13455150-13455627 | Common:5; Rare:188 | ||||
| chr3:13476174-13476443 | Common:4; Rare:71 | ||||
| chr3:13485170-13485480 | Rare:69 | ||||
| chr3:13502441-13502841 | Common:6; Rare:96 | ||||
| chr3:13507650-13508140 | Common:1; Rare:132 | ||||
| chr3:13513512-13513690 | Common:1; Rare:41 | ||||
| chr3:13514147-13514524 | Common:6; Rare:99 | ||||
| chr3:13533713-13534100 | Common:6; Rare:133 | ||||
| chr3:13537880-13538280 | Common:4; Rare:84 | ||||
| chr3:13895300-13895670 | Common:1; Rare:152 | ||||
| chr3:13962893-13963573 | Common:7; Rare:208 | ||||
| chr3:13965767-13966470 | Common:13; Rare:286 | ||||
| chr3:14144427-14145349 | Common:17; Rare:292; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:14224990-14225450 | Common:3; Rare:105 |