| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:79018590-79018920 | Common:2; Rare:124 | ||||
| chr3:79018973-79019180 | Rare:140 | ||||
| chr3:79019335-79019471 | Common:1; Rare:41 | ||||
| chr3:79019389-79019556 | Common:3; Rare:55 | ||||
| chr3:81761160-81762243 | Common:22; Rare:526; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr3:84958725-84959052 | Common:8; Rare:183 | ||||
| chr3:86990760-86991100 | Common:1; Rare:82 | ||||
| chr3:86991120-86991700 | Common:1; Rare:121 | ||||
| chr3:87227067-87227445 | Common:5; Rare:242; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:87227526-87227978 | Common:2; Rare:121; Clinvar (benign):2 | ||||
| chr3:88058609-88058821 | Common:2; Rare:111 | ||||
| chr3:88058824-88059408 | Common:12; Rare:568 | ||||
| chr3:88149079-88149281 | Common:1; Rare:56 | ||||
| chr3:88149570-88150106 | Common:14; Rare:416 | ||||
| chr3:93973270-93973740 | Common:1; Rare:154; Clinvar (benign):2 |