| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32685266-32685394 | Rare:30 | ||||
| chr3:33097090-33097265 | Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33440946-33441039 | Rare:11 | ||||
| chr3:33718061-33718314 | Rare:95 | ||||
| chr3:33798520-33798686 | Common:2; Rare:60 | ||||
| chr3:33798985-33799203 | Rare:68 | ||||
| chr3:36908433-36908613 | Common:1; Rare:37 | ||||
| chr3:36944855-36945116 | Common:1; Rare:59 | ||||
| chr3:36993067-36993557 | Common:2; Rare:167; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37175840-37175931 | Rare:21 | ||||
| chr3:37176078-37176651 | Common:2; Rare:163 | ||||
| chr3:37243122-37243474 | Common:3; Rare:92 | ||||
| chr3:37998991-37999294 | Common:3; Rare:86 | ||||
| chr3:38024464-38024667 | Common:1; Rare:79 | ||||
| chr3:38137108-38137389 | Rare:58 |