| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:87227231-87227382 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058932-88059294 | Common:3; Rare:133 | ||||
| chr3:88149605-88149682 | Common:1; Rare:19 | ||||
| chr3:88149856-88150043 | Common:5; Rare:75 | ||||
| chr3:94062977-94063080 | Rare:19 | ||||
| chr3:97764496-97764802 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821890-97822179 | Common:2; Rare:97 | ||||
| chr3:98732445-98732559 | Rare:18 | ||||
| chr3:98732640-98732717 | Rare:19 | ||||
| chr3:99638328-99638658 | Common:1; Rare:72 | ||||
| chr3:99638825-99639086 | Common:2; Rare:44 | ||||
| chr3:99817566-99817928 | Rare:107 | ||||
| chr3:99850941-99851194 | Rare:65 | ||||
| chr3:99876096-99876278 | Common:1; Rare:50 | ||||
| chr3:100260753-100261042 | Rare:79 |