| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58558890-58559136 | Common:1; Rare:79 | ||||
| chr19:58573486-58573575 | Common:1; Rare:23 | ||||
| chr2:264006-264137 | Common:2; Rare:45 | ||||
| chr2:264799-265006 | Common:1; Rare:111 | ||||
| chr2:677358-677493 | Common:1; Rare:56 | ||||
| chr2:3377811-3378028 | Common:2; Rare:61 | ||||
| chr2:3379600-3379808 | Common:2; Rare:82 | ||||
| chr2:3519370-3519659 | Common:2; Rare:85 | ||||
| chr2:3558244-3558695 | Common:6; Rare:169 | ||||
| chr2:3575070-3575385 | Common:3; Rare:93; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9423148-9423676 | Common:1; Rare:139 | ||||
| chr2:9474500-9474630 | Common:6; Rare:62 | ||||
| chr2:9488068-9488171 | Rare:28 | ||||
| chr2:9555712-9555903 | Common:2; Rare:64 | ||||
| chr2:10302426-10302610 | Rare:57 |