| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:29280565-29280602 | Common:1; Rare:5 | ||||
| chr3:29280810-29280848 | Rare:8 | ||||
| chr3:29280871-29281104 | Common:2; Rare:46 | ||||
| chr3:29281277-29281690 | Common:3; Rare:94 | ||||
| chr3:30606291-30606804 | Common:2; Rare:144; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:31532381-31532638 | Common:2; Rare:71 | ||||
| chr3:31532764-31532994 | Common:3; Rare:93 | ||||
| chr3:31981225-31981439 | Common:2; Rare:43 | ||||
| chr3:33096755-33097050 | Common:1; Rare:90; Clinvar:1; Clinvar (pathogenic):4 | ||||
| chr3:33277334-33277497 | Common:1; Rare:46 | ||||
| chr3:33798484-33798716 | Common:2; Rare:84 | ||||
| chr3:33798975-33799120 | Rare:49 | ||||
| chr3:36993057-36993611 | Common:2; Rare:196; Clinvar:39; Clinvar (benign):18; Clinvar (pathogenic):4 | ||||
| chr3:36993663-36993835 | Rare:71; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:37176061-37176398 | Common:1; Rare:95 |