| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:67654583-67654825 | Common:2; Rare:85 | ||||
| chr3:69052216-69052429 | Common:4; Rare:75 | ||||
| chr3:69200480-69200685 | Common:2; Rare:29 | ||||
| chr3:69200881-69200985 | Common:1; Rare:24 | ||||
| chr3:72848376-72848517 | Rare:53 | ||||
| chr3:72996720-72997040 | Common:1; Rare:120 | ||||
| chr3:79018974-79019055 | Rare:26 | ||||
| chr3:87227185-87227382 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058884-88059322 | Common:3; Rare:172 | ||||
| chr3:88149649-88149764 | Rare:24 | ||||
| chr3:88149851-88150049 | Common:5; Rare:77 | ||||
| chr3:93979912-93980231 | Common:4; Rare:122; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94062867-94063101 | Rare:60 | ||||
| chr3:97764458-97764802 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821902-97822180 | Common:2; Rare:97 |