| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:27484302-27484735 | Common:8; Rare:275 | ||||
| chr3:28241439-28241791 | Common:4; Rare:238 | ||||
| chr3:28348460-28349185 | Common:7; Rare:373 | ||||
| chr3:30606223-30607199 | Common:6; Rare:462; Clinvar:18; Clinvar (benign):14 | ||||
| chr3:31531990-31532220 | Common:8; Rare:105 | ||||
| chr3:31532371-31532777 | Common:5; Rare:123 | ||||
| chr3:31532790-31533008 | Common:4; Rare:165 | ||||
| chr3:31981220-31981449 | Common:4; Rare:88 | ||||
| chr3:31981595-31981816 | Common:1; Rare:97 | ||||
| chr3:32077528-32077819 | Common:5; Rare:95 | ||||
| chr3:32106323-32106689 | Common:4; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32238560-32238805 | Common:2; Rare:63 | ||||
| chr3:32391739-32391962 | Common:6; Rare:117 | ||||
| chr3:32502779-32502928 | Rare:81 | ||||
| chr3:32570157-32570375 | Common:3; Rare:147 |