| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28348777-28349350 | Common:9; Rare:331 | ||||
| chr3:29280855-29281073 | Common:3; Rare:42 | ||||
| chr3:30606404-30606757 | Common:3; Rare:154; Clinvar:7; Clinvar (benign):3 | ||||
| chr3:31531920-31532180 | Common:9; Rare:114 | ||||
| chr3:31532350-31532745 | Common:8; Rare:230 | ||||
| chr3:31532800-31533023 | Common:4; Rare:171 | ||||
| chr3:31981210-31981444 | Common:4; Rare:93 | ||||
| chr3:31981503-31981884 | Common:3; Rare:130 | ||||
| chr3:32106392-32106709 | Common:8; Rare:170; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:32502779-32502891 | Rare:38 | ||||
| chr3:32569910-32570530 | Common:5; Rare:281 | ||||
| chr3:32570752-32570980 | Common:2; Rare:186 | ||||
| chr3:32685079-32685397 | Rare:183 | ||||
| chr3:33096741-33096867 | Rare:38 | ||||
| chr3:33097017-33097296 | Common:5; Rare:165; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):1 |