| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32685074-32685409 | Rare:99 | ||||
| chr3:33277294-33277512 | Common:3; Rare:66 | ||||
| chr3:33645228-33645538 | Rare:55 | ||||
| chr3:33658979-33659065 | Rare:21 | ||||
| chr3:33659505-33659647 | Rare:28 | ||||
| chr3:33798512-33798686 | Common:2; Rare:62 | ||||
| chr3:35639192-35639747 | Common:4; Rare:131 | ||||
| chr3:35639968-35640033 | Rare:13 | ||||
| chr3:35642164-35642356 | Rare:26 | ||||
| chr3:36993051-36993559 | Common:2; Rare:175; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37176140-37176393 | Rare:68 | ||||
| chr3:37243166-37243348 | Common:1; Rare:48 | ||||
| chr3:38024470-38024664 | Common:1; Rare:74 | ||||
| chr3:38029640-38029864 | Common:1; Rare:45 | ||||
| chr3:39051942-39052073 | Common:1; Rare:50 |