| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31722495-31722677 | Rare:40 | ||||
| chr20:31722778-31722962 | Rare:47 | ||||
| chr20:31739085-31739413 | Common:2; Rare:86 | ||||
| chr20:32207712-32207939 | Common:3; Rare:86 | ||||
| chr20:32483456-32483812 | Common:1; Rare:56 | ||||
| chr20:33401461-33401618 | Rare:40 | ||||
| chr20:33720262-33720542 | Common:4; Rare:62 | ||||
| chr20:33993058-33993275 | Common:1; Rare:59 | ||||
| chr20:33993672-33994125 | Common:3; Rare:152 | ||||
| chr20:34112094-34112427 | Rare:108 | ||||
| chr20:34302956-34303337 | Common:1; Rare:143; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:34516330-34516451 | Rare:50 | ||||
| chr20:34677057-34677290 | Rare:67 | ||||
| chr20:34876289-34876643 | Common:3; Rare:100 | ||||
| chr20:34955725-34955827 | Common:1; Rare:38; Clinvar:3; Clinvar (benign):3 |