| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28348600-28348711 | Rare:24 | ||||
| chr3:28348779-28349185 | Common:3; Rare:128 | ||||
| chr3:29280837-29281081 | Common:3; Rare:49 | ||||
| chr3:31532391-31532662 | Common:4; Rare:77 | ||||
| chr3:31533016-31533293 | Common:1; Rare:89; Clinvar (benign):2 | ||||
| chr3:32570655-32570956 | Common:1; Rare:136 | ||||
| chr3:33097104-33097265 | Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277313-33277476 | Common:1; Rare:41 | ||||
| chr3:33798296-33798701 | Common:2; Rare:117 | ||||
| chr3:33798985-33799203 | Rare:68 | ||||
| chr3:35639441-35639848 | Common:4; Rare:87 | ||||
| chr3:35639850-35640056 | Common:2; Rare:45 | ||||
| chr3:36992827-36992939 | Rare:26 | ||||
| chr3:36993077-36993563 | Common:2; Rare:165; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37176237-37176393 | Rare:51 |