| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69084812-69085063 | Common:3; Rare:71 | ||||
| chr3:69542568-69542804 | Common:2; Rare:70 | ||||
| chr3:71583668-71583775 | Rare:36 | ||||
| chr3:71725219-71725514 | Common:2; Rare:108 | ||||
| chr3:71753570-71753827 | Common:4; Rare:104 | ||||
| chr3:71755062-71755346 | Rare:68 | ||||
| chr3:73624869-73625069 | Common:3; Rare:64 | ||||
| chr3:75785533-75785731 | Common:4; Rare:24 | ||||
| chr3:79018999-79019106 | Rare:31 | ||||
| chr3:79767973-79768197 | Rare:29 | ||||
| chr3:84958802-84959179 | Common:4; Rare:116 | ||||
| chr3:84959291-84959388 | Common:1; Rare:22 | ||||
| chr3:84959641-84959816 | Rare:48 | ||||
| chr3:86991109-86991426 | Common:1; Rare:81 | ||||
| chr3:87227245-87227512 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):3 |