| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38029600-38029844 | Common:1; Rare:49 | ||||
| chr3:38138549-38138698 | Common:2; Rare:58; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:39051939-39052072 | Common:1; Rare:50 | ||||
| chr3:39107574-39107716 | Common:3; Rare:44 | ||||
| chr3:39153550-39153730 | Common:3; Rare:60 | ||||
| chr3:39383324-39383439 | Common:2; Rare:23; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383582-39383676 | Rare:20; Clinvar:1 | ||||
| chr3:40309471-40309903 | Common:9; Rare:142 | ||||
| chr3:40524815-40525004 | Common:1; Rare:54 | ||||
| chr3:41962305-41962562 | Common:2; Rare:66 | ||||
| chr3:42581909-42582132 | Common:3; Rare:67 | ||||
| chr3:42582256-42582338 | Rare:23 | ||||
| chr3:42600545-42600757 | Rare:85 | ||||
| chr3:42600917-42600994 | Rare:31 | ||||
| chr3:42773215-42773357 | Common:1; Rare:37 |