| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:63911984-63912116 | Rare:41 | ||||
| chr3:64687587-64687722 | Rare:36 | ||||
| chr3:64687987-64688109 | Rare:34 | ||||
| chr3:66038553-66038642 | Rare:21 | ||||
| chr3:66997989-66998312 | Rare:80 | ||||
| chr3:67654562-67654727 | Common:1; Rare:64 | ||||
| chr3:69013214-69013403 | Rare:54 | ||||
| chr3:69013590-69013746 | Rare:41 | ||||
| chr3:69084776-69085221 | Common:3; Rare:115 | ||||
| chr3:69542534-69542725 | Common:3; Rare:51 | ||||
| chr3:71130549-71130672 | Rare:48; Clinvar:2 | ||||
| chr3:73556904-73557198 | Common:4; Rare:55 | ||||
| chr3:79018959-79019108 | Rare:41 | ||||
| chr3:81743075-81743172 | Common:1; Rare:18 | ||||
| chr3:81761389-81761813 | Common:8; Rare:153; Clinvar:2; Clinvar (benign):4 |