| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15099056-15099460 | Common:2; Rare:100 | ||||
| chr3:15205900-15206300 | Common:1; Rare:135 | ||||
| chr3:15332479-15332704 | Common:2; Rare:62 | ||||
| chr3:15427282-15427730 | Common:1; Rare:129 | ||||
| chr3:15601262-15601357 | Common:1; Rare:32 | ||||
| chr3:15601476-15602085 | Common:6; Rare:273; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:15797934-15797985 | Rare:8 | ||||
| chr3:15798139-15798267 | Common:1; Rare:37 | ||||
| chr3:15858936-15858986 | Rare:8 | ||||
| chr3:15859006-15859183 | Common:1; Rare:56 | ||||
| chr3:15859522-15859688 | Common:4; Rare:46 | ||||
| chr3:15859793-15859940 | Common:1; Rare:35 | ||||
| chr3:15860038-15860098 | Common:1; Rare:12 | ||||
| chr3:15860137-15860444 | Common:1; Rare:61 | ||||
| chr3:16264602-16264762 | Common:1; Rare:53 |