| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57889856-57890079 | Common:1; Rare:46; Clinvar (benign):2 | ||||
| chr3:58008350-58008696 | Common:1; Rare:114; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:58149910-58150217 | Rare:108; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:58433774-58433952 | Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:58491951-58492147 | Common:2; Rare:49 | ||||
| chr3:58537157-58537240 | Common:1; Rare:21 | ||||
| chr3:59049980-59050173 | Common:1; Rare:63 | ||||
| chr3:61251400-61251594 | Common:4; Rare:51 | ||||
| chr3:61561412-61561655 | Common:2; Rare:85 | ||||
| chr3:62318881-62319055 | Rare:73 | ||||
| chr3:63863777-63864158 | Common:8; Rare:127 | ||||
| chr3:64687594-64687753 | Rare:40 | ||||
| chr3:67654582-67654722 | Common:1; Rare:48 | ||||
| chr3:68932537-68932713 | Common:1; Rare:53 | ||||
| chr3:69013208-69013407 | Rare:55 |