| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57556006-57556321 | Rare:76 | ||||
| chr3:57597250-57597661 | Common:4; Rare:130 | ||||
| chr3:58008252-58008461 | Common:2; Rare:82; Clinvar:2 | ||||
| chr3:58433769-58433928 | Rare:69; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:61561434-61561583 | Common:1; Rare:50 | ||||
| chr3:62318925-62319055 | Rare:52 | ||||
| chr3:62875361-62875484 | Common:1; Rare:26 | ||||
| chr3:63863785-63864158 | Common:8; Rare:126 | ||||
| chr3:63864427-63864464 | Common:1; Rare:11 | ||||
| chr3:67654582-67654722 | Common:1; Rare:48 | ||||
| chr3:69013208-69013415 | Rare:58 | ||||
| chr3:69013590-69014001 | Common:2; Rare:137 | ||||
| chr3:69052208-69052437 | Common:4; Rare:80 | ||||
| chr3:69084758-69085063 | Common:3; Rare:78 | ||||
| chr3:69200497-69200550 | Rare:7 |