| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57597324-57597737 | Common:4; Rare:124 | ||||
| chr3:58433810-58433965 | Rare:61; Clinvar (benign):2 | ||||
| chr3:61251390-61251593 | Common:4; Rare:52 | ||||
| chr3:62318890-62319049 | Rare:67 | ||||
| chr3:63863786-63864114 | Common:7; Rare:111 | ||||
| chr3:67654567-67654796 | Common:2; Rare:87 | ||||
| chr3:69013588-69013812 | Common:1; Rare:68 | ||||
| chr3:69320944-69321184 | Rare:40 | ||||
| chr3:73624149-73624574 | Common:5; Rare:127 | ||||
| chr3:81761523-81761781 | Common:8; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:88058935-88059294 | Common:2; Rare:133 | ||||
| chr3:88149851-88150033 | Common:2; Rare:62 | ||||
| chr3:94062918-94063017 | Rare:29 | ||||
| chr3:97764472-97764548 | Rare:15 | ||||
| chr3:97764706-97764805 | Common:1; Rare:22; Clinvar:1; Clinvar (benign):1 |