| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:88149856-88150055 | Common:5; Rare:79 | ||||
| chr3:94028580-94028733 | Rare:28 | ||||
| chr3:94062897-94063093 | Rare:47 | ||||
| chr3:96814328-96814638 | Rare:107 | ||||
| chr3:97764485-97764605 | Rare:20 | ||||
| chr3:97764658-97764813 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821858-97822216 | Common:2; Rare:125 | ||||
| chr3:97972358-97972522 | Common:3; Rare:66 | ||||
| chr3:98522601-98522683 | Rare:19 | ||||
| chr3:98732427-98732589 | Rare:27 | ||||
| chr3:98732619-98732733 | Rare:23 | ||||
| chr3:99638416-99638746 | Common:1; Rare:79 | ||||
| chr3:99638758-99639000 | Common:1; Rare:39 | ||||
| chr3:99817560-99817928 | Rare:111 | ||||
| chr3:99876096-99876278 | Common:1; Rare:50 |