| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32106431-32106714 | Common:3; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502747-32502902 | Rare:53 | ||||
| chr3:32570636-32570956 | Common:1; Rare:144 | ||||
| chr3:32685051-32685372 | Rare:99 | ||||
| chr3:33097098-33097265 | Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33218786-33218822 | Rare:12 | ||||
| chr3:33277261-33277513 | Common:3; Rare:73 | ||||
| chr3:33645183-33645549 | Rare:62 | ||||
| chr3:33658979-33659443 | Common:3; Rare:84 | ||||
| chr3:33659506-33659776 | Common:1; Rare:64 | ||||
| chr3:33798472-33798686 | Common:2; Rare:77 | ||||
| chr3:35638730-35638951 | Rare:47 | ||||
| chr3:35639434-35639838 | Common:4; Rare:89 | ||||
| chr3:35639858-35639895 | Rare:7 | ||||
| chr3:35639910-35640098 | Common:2; Rare:44 |