| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:61561412-61561656 | Common:2; Rare:86 | ||||
| chr3:62318890-62319055 | Rare:69 | ||||
| chr3:63863771-63864158 | Common:8; Rare:129 | ||||
| chr3:66038472-66038656 | Rare:41 | ||||
| chr3:66998010-66998356 | Common:2; Rare:86 | ||||
| chr3:67654502-67654861 | Common:2; Rare:138 | ||||
| chr3:69013231-69013288 | Rare:13 | ||||
| chr3:69013590-69013790 | Common:1; Rare:58 | ||||
| chr3:69084847-69085066 | Common:3; Rare:62 | ||||
| chr3:69200867-69201021 | Common:1; Rare:36 | ||||
| chr3:71130550-71130685 | Rare:57; Clinvar:2 | ||||
| chr3:72848370-72848580 | Common:1; Rare:73 | ||||
| chr3:79018806-79018991 | Common:1; Rare:45 | ||||
| chr3:87227189-87227395 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058926-88059336 | Common:3; Rare:154 |