| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58554945-58555266 | Common:2; Rare:112 | ||||
| chr19:58558310-58558675 | Rare:116 | ||||
| chr19:58558897-58559150 | Common:1; Rare:78 | ||||
| chr19:58573290-58573742 | Common:4; Rare:115 | ||||
| chr2:45784-45940 | Rare:64 | ||||
| chr2:264013-264088 | Common:1; Rare:27 | ||||
| chr2:677358-677564 | Common:1; Rare:87 | ||||
| chr2:1373662-1374028 | Common:4; Rare:87 | ||||
| chr2:1654399-1654590 | Rare:58 | ||||
| chr2:1744447-1744688 | Common:2; Rare:84 | ||||
| chr2:3377791-3377953 | Rare:43 | ||||
| chr2:3379653-3379795 | Common:2; Rare:61 | ||||
| chr2:3519458-3519660 | Common:2; Rare:62 | ||||
| chr2:3558208-3558565 | Common:6; Rare:140 | ||||
| chr2:3575114-3575448 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):6 |