| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:87227237-87227400 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058917-88059294 | Common:3; Rare:141 | ||||
| chr3:88149659-88149698 | Rare:7 | ||||
| chr3:88149851-88150055 | Common:5; Rare:79 | ||||
| chr3:94062904-94063093 | Rare:45 | ||||
| chr3:97764496-97764833 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821687-97822102 | Rare:129 | ||||
| chr3:98732445-98732506 | Rare:13 | ||||
| chr3:99638328-99638580 | Common:1; Rare:55 | ||||
| chr3:99638583-99638633 | Rare:9 | ||||
| chr3:99817568-99817920 | Rare:102 | ||||
| chr3:99876091-99876278 | Common:1; Rare:51 | ||||
| chr3:100260733-100261034 | Rare:79 | ||||
| chr3:100401378-100401582 | Common:1; Rare:45 | ||||
| chr3:100492445-100492744 | Common:2; Rare:87 |