| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:56557065-56557234 | Common:2; Rare:69 | ||||
| chr3:57079252-57079464 | Common:2; Rare:69 | ||||
| chr3:57227598-57227913 | Common:3; Rare:108 | ||||
| chr3:57555987-57556321 | Rare:86 | ||||
| chr3:57597330-57597737 | Common:4; Rare:123 | ||||
| chr3:58433814-58434029 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr3:61561412-61561583 | Common:1; Rare:65 | ||||
| chr3:62318888-62319069 | Rare:75 | ||||
| chr3:63863777-63864125 | Common:7; Rare:116 | ||||
| chr3:65597443-65597624 | Rare:37 | ||||
| chr3:67654569-67654754 | Common:2; Rare:74 | ||||
| chr3:69013630-69013998 | Common:2; Rare:128 | ||||
| chr3:69052219-69052397 | Common:3; Rare:74 | ||||
| chr3:69080349-69080456 | Rare:44 | ||||
| chr3:69084762-69085051 | Common:3; Rare:71 |