| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:79018874-79019069 | Rare:49 | ||||
| chr3:81761616-81761828 | Common:3; Rare:69; Clinvar:1 | ||||
| chr3:87227186-87227477 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058178-88058723 | Common:2; Rare:151 | ||||
| chr3:88058923-88059322 | Common:3; Rare:152 | ||||
| chr3:88149642-88149758 | Rare:24 | ||||
| chr3:88149840-88150055 | Common:5; Rare:81 | ||||
| chr3:94062887-94062970 | Rare:28 | ||||
| chr3:94062977-94063083 | Rare:20 | ||||
| chr3:97764488-97764814 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821902-97822107 | Rare:74 | ||||
| chr3:98522601-98522746 | Rare:33 | ||||
| chr3:98732422-98732512 | Rare:17 | ||||
| chr3:98732617-98732725 | Rare:22 | ||||
| chr3:98901656-98901998 | Common:1; Rare:129 |