| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:58108901-58109321 | Common:2; Rare:104; Clinvar:3 | ||||
| chr3:58109989-58110439 | Common:1; Rare:118; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:58111816-58112290 | Common:1; Rare:113; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:58114480-58114692 | Common:3; Rare:36 | ||||
| chr3:58117090-58117332 | Common:2; Rare:43 | ||||
| chr3:58118658-58118911 | Rare:48; Clinvar (benign):1 | ||||
| chr3:58120956-58121317 | Rare:87; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:58124310-58124766 | Common:6; Rare:132; Clinvar:3; Clinvar (benign):4 | ||||
| chr3:58134408-58134628 | Rare:41; Clinvar (benign):1 | ||||
| chr3:58134740-58135003 | Common:2; Rare:57; Clinvar (benign):1 | ||||
| chr3:58141820-58141955 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:58144091-58144252 | Rare:26 | ||||
| chr3:58159551-58159895 | Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:58161076-58161360 | Common:3; Rare:51 | ||||
| chr3:58162231-58162447 | Common:2; Rare:34 |