| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:61251383-61251594 | Common:4; Rare:53 | ||||
| chr3:61561412-61561662 | Common:2; Rare:89 | ||||
| chr3:62318894-62319076 | Rare:75 | ||||
| chr3:63863773-63864167 | Common:8; Rare:130 | ||||
| chr3:63911996-63912105 | Rare:36 | ||||
| chr3:64687578-64687788 | Common:1; Rare:54 | ||||
| chr3:64687987-64688188 | Common:1; Rare:58 | ||||
| chr3:67654561-67654778 | Common:2; Rare:86 | ||||
| chr3:69013208-69013334 | Rare:34 | ||||
| chr3:69013580-69013756 | Rare:46 | ||||
| chr3:69084762-69085073 | Common:3; Rare:78 | ||||
| chr3:70977645-70977913 | Rare:90; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:71581834-71582155 | Common:1; Rare:73 | ||||
| chr3:72996672-72997030 | Common:2; Rare:140 | ||||
| chr3:73624154-73624454 | Common:5; Rare:94 |