| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28348779-28348861 | Common:1; Rare:26 | ||||
| chr3:28348905-28349178 | Common:2; Rare:96 | ||||
| chr3:29280831-29281081 | Common:3; Rare:49 | ||||
| chr3:31532380-31532656 | Common:4; Rare:77 | ||||
| chr3:32238536-32238730 | Common:2; Rare:61 | ||||
| chr3:32502775-32502910 | Rare:42 | ||||
| chr3:32570655-32570895 | Rare:110 | ||||
| chr3:33798520-33798692 | Common:2; Rare:63 | ||||
| chr3:36993112-36993564 | Common:2; Rare:143; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37243032-37243474 | Common:5; Rare:115 | ||||
| chr3:38024453-38024652 | Common:1; Rare:75 | ||||
| chr3:38137114-38137447 | Common:1; Rare:74 | ||||
| chr3:38138597-38138811 | Common:2; Rare:79; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:39051950-39052050 | Common:1; Rare:36 | ||||
| chr3:39107555-39107716 | Common:3; Rare:50 |