| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:8501644-8501854 | Rare:73 | ||||
| chr3:8963427-8963787 | Common:2; Rare:85 | ||||
| chr3:9249593-9249742 | Common:1; Rare:36 | ||||
| chr3:9363001-9363098 | Rare:34 | ||||
| chr3:9397434-9397673 | Rare:79 | ||||
| chr3:9397777-9397873 | Rare:20 | ||||
| chr3:9792737-9793115 | Common:3; Rare:129 | ||||
| chr3:9890474-9890646 | Common:1; Rare:64 | ||||
| chr3:9933507-9933877 | Common:2; Rare:149; Clinvar:3 | ||||
| chr3:10026315-10026455 | Rare:45 | ||||
| chr3:10115515-10115712 | Common:4; Rare:70 | ||||
| chr3:10141695-10141991 | Common:1; Rare:143; Clinvar:38; Clinvar (benign):32 | ||||
| chr3:11272236-11272413 | Common:1; Rare:36 | ||||
| chr3:11719442-11719595 | Rare:50 | ||||
| chr3:12004250-12004393 | Common:2; Rare:43 |