| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32106441-32106714 | Common:3; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502779-32502924 | Rare:43 | ||||
| chr3:32570666-32570925 | Rare:118 | ||||
| chr3:33097103-33097286 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277313-33277482 | Common:1; Rare:45 | ||||
| chr3:33718021-33718295 | Rare:99 | ||||
| chr3:33798472-33798681 | Common:2; Rare:74 | ||||
| chr3:33799014-33799029 | Rare:6 | ||||
| chr3:36993113-36993544 | Common:2; Rare:135; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr3:37176140-37176393 | Rare:68 | ||||
| chr3:37243166-37243565 | Common:1; Rare:107 | ||||
| chr3:38024501-38024667 | Common:1; Rare:64 | ||||
| chr3:38029616-38029864 | Common:1; Rare:50 | ||||
| chr3:38125694-38125916 | Common:1; Rare:72 | ||||
| chr3:39051962-39052032 | Common:1; Rare:24 |