| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32063362-32063699 | Common:1; Rare:119; Clinvar:1 | ||||
| chr2:32165665-32165903 | Common:1; Rare:96 | ||||
| chr2:32277765-32277940 | Common:1; Rare:44 | ||||
| chr2:32356911-32357192 | Common:4; Rare:121 | ||||
| chr2:32627937-32628157 | Rare:68 | ||||
| chr2:33134417-33134617 | Common:2; Rare:40 | ||||
| chr2:33476503-33476688 | Common:2; Rare:33 | ||||
| chr2:33599222-33599588 | Common:1; Rare:129 | ||||
| chr2:37084276-37084565 | Common:3; Rare:110 | ||||
| chr2:37156912-37157050 | Common:1; Rare:43 | ||||
| chr2:37231525-37231745 | Common:4; Rare:129; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:37323755-37323945 | Common:5; Rare:48 | ||||
| chr2:37324681-37324972 | Common:1; Rare:109 | ||||
| chr2:37344147-37344462 | Common:6; Rare:67 | ||||
| chr2:37344464-37344850 | Common:2; Rare:131 |