| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12484158-12484554 | Common:5; Rare:115; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12556760-12557139 | Common:5; Rare:104 | ||||
| chr3:12664064-12664321 | Common:2; Rare:72; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:13420231-13420458 | Common:1; Rare:65 | ||||
| chr3:13480040-13480334 | Common:2; Rare:69 | ||||
| chr3:14124746-14125147 | Common:4; Rare:116; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178880 | Common:2; Rare:165; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402428-14402632 | Rare:52 | ||||
| chr3:14651486-14651832 | Rare:107 | ||||
| chr3:14947204-14947563 | Common:4; Rare:158 | ||||
| chr3:14948398-14948648 | Common:2; Rare:75 | ||||
| chr3:15065204-15065399 | Common:2; Rare:78 | ||||
| chr3:15099109-15099293 | Rare:46 | ||||
| chr3:15206057-15206322 | Common:1; Rare:103 | ||||
| chr3:15427459-15427741 | Common:1; Rare:96 |