| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69084767-69085201 | Common:3; Rare:109 | ||||
| chr3:69200491-69200679 | Common:1; Rare:27 | ||||
| chr3:69200880-69201008 | Common:1; Rare:28 | ||||
| chr3:69542323-69542401 | Rare:13 | ||||
| chr3:69542563-69542742 | Common:2; Rare:46 | ||||
| chr3:69866167-69866284 | Rare:21 | ||||
| chr3:71130527-71130655 | Rare:48; Clinvar:2 | ||||
| chr3:72848376-72848580 | Common:1; Rare:70 | ||||
| chr3:72996715-72997067 | Common:2; Rare:127 | ||||
| chr3:77039987-77040150 | Common:1; Rare:42 | ||||
| chr3:81761459-81761773 | Common:8; Rare:116; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:87227189-87227413 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058926-88059313 | Common:3; Rare:144 | ||||
| chr3:88149648-88150055 | Common:5; Rare:125 | ||||
| chr3:93973750-93973981 | Rare:77; Clinvar:5 |