| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:11136860-11137271 | Rare:82 | ||||
| chr3:11154346-11154542 | Common:3; Rare:51 | ||||
| chr3:11643811-11643952 | Rare:41 | ||||
| chr3:11643960-11643995 | Common:2; Rare:5 | ||||
| chr3:11719419-11719595 | Rare:57 | ||||
| chr3:12158848-12158990 | Rare:47 | ||||
| chr3:12663963-12664330 | Common:2; Rare:103; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:13480076-13480339 | Common:1; Rare:63 | ||||
| chr3:13548969-13549185 | Common:1; Rare:70 | ||||
| chr3:14124738-14125202 | Common:4; Rare:137; Clinvar:8; Clinvar (benign):2 | ||||
| chr3:14135568-14135905 | Common:2; Rare:97; Clinvar:6; Clinvar (benign):5 | ||||
| chr3:14178564-14178880 | Common:2; Rare:165; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402457-14402632 | Rare:45 | ||||
| chr3:14651483-14651860 | Rare:117 | ||||
| chr3:14947209-14947563 | Common:4; Rare:156 |