| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:88058893-88059350 | Common:3; Rare:178 | ||||
| chr3:88149605-88149776 | Common:1; Rare:41 | ||||
| chr3:88149862-88150174 | Common:6; Rare:118 | ||||
| chr3:94062794-94062890 | Common:1; Rare:20 | ||||
| chr3:94062901-94063083 | Rare:45 | ||||
| chr3:97764492-97764793 | Common:1; Rare:65; Clinvar (benign):1 | ||||
| chr3:97821876-97822070 | Rare:74 | ||||
| chr3:97972382-97972616 | Common:6; Rare:67 | ||||
| chr3:98522844-98523098 | Common:1; Rare:77 | ||||
| chr3:98593145-98593369 | Common:1; Rare:80; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:98732431-98732718 | Rare:53 | ||||
| chr3:98800579-98800931 | Common:1; Rare:74 | ||||
| chr3:98812505-98812655 | Common:1; Rare:26 | ||||
| chr3:98812790-98812868 | Rare:6 | ||||
| chr3:98816031-98816297 | Common:1; Rare:41 |