| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27212231-27212371 | Common:1; Rare:73 | ||||
| chr2:27217319-27217432 | Rare:54 | ||||
| chr2:27323040-27323145 | Rare:29; Clinvar (benign):1 | ||||
| chr2:27356750-27356863 | Rare:30 | ||||
| chr2:27356961-27357205 | Common:2; Rare:90 | ||||
| chr2:27369181-27369258 | Rare:21; Clinvar:1 | ||||
| chr2:27370257-27370648 | Common:1; Rare:160 | ||||
| chr2:27380522-27380891 | Common:2; Rare:136; Clinvar:7 | ||||
| chr2:27442215-27442436 | Common:1; Rare:85 | ||||
| chr2:27582975-27583122 | Rare:54 | ||||
| chr2:27628981-27629055 | Common:1; Rare:37 | ||||
| chr2:27663358-27663469 | Rare:30 | ||||
| chr2:27663541-27663934 | Rare:146 | ||||
| chr2:27664041-27664548 | Common:2; Rare:173 | ||||
| chr2:27890320-27890498 | Common:2; Rare:58 |