| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:16512900-16513026 | Common:1; Rare:20 | ||||
| chr3:16513497-16513835 | Common:4; Rare:77 | ||||
| chr3:17742596-17742946 | Common:4; Rare:121 | ||||
| chr3:20186139-20186415 | Common:4; Rare:90 | ||||
| chr3:23916905-23917205 | Rare:115 | ||||
| chr3:25428107-25428284 | Rare:33 | ||||
| chr3:25790008-25790118 | Common:3; Rare:42 | ||||
| chr3:29280843-29281081 | Common:3; Rare:45 | ||||
| chr3:31532391-31532675 | Common:4; Rare:83 | ||||
| chr3:32106378-32106690 | Common:4; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32570766-32570948 | Common:1; Rare:85 | ||||
| chr3:33097090-33097234 | Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277325-33277487 | Common:1; Rare:42 | ||||
| chr3:36993166-36993563 | Common:2; Rare:119; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:39107597-39107681 | Common:2; Rare:26 |