| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:79018992-79019108 | Rare:35 | ||||
| chr3:79019413-79019556 | Common:3; Rare:46 | ||||
| chr3:81761642-81761702 | Rare:21 | ||||
| chr3:87227032-87227424 | Common:3; Rare:113; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058186-88058498 | Common:1; Rare:78 | ||||
| chr3:88058923-88059308 | Common:3; Rare:144 | ||||
| chr3:88149599-88149758 | Common:1; Rare:37 | ||||
| chr3:88149807-88150055 | Common:5; Rare:86 | ||||
| chr3:93979918-93980236 | Common:4; Rare:122; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94062870-94063097 | Rare:59 | ||||
| chr3:96814380-96814586 | Rare:73 | ||||
| chr3:97764423-97764608 | Rare:40 | ||||
| chr3:97764676-97764802 | Common:1; Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821885-97822074 | Rare:70 | ||||
| chr3:97972390-97972538 | Common:3; Rare:54 |