| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42600320-42600778 | Common:3; Rare:175 | ||||
| chr3:42600905-42601009 | Rare:43 | ||||
| chr3:42773211-42773345 | Common:1; Rare:38 | ||||
| chr3:42804401-42804684 | Common:2; Rare:91 | ||||
| chr3:43286431-43286654 | Common:2; Rare:97 | ||||
| chr3:43621841-43622175 | Common:2; Rare:110; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690811-43691023 | Common:4; Rare:117; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:44338067-44338193 | Common:2; Rare:44 | ||||
| chr3:44338319-44338506 | Common:3; Rare:61 | ||||
| chr3:44338667-44338818 | Common:3; Rare:54 | ||||
| chr3:44477609-44477780 | Common:1; Rare:44 | ||||
| chr3:44510544-44510929 | Common:8; Rare:99 | ||||
| chr3:44555121-44555274 | Rare:36 | ||||
| chr3:44584699-44584998 | Rare:55 | ||||
| chr3:44624839-44625109 | Common:2; Rare:74 |