| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58558893-58559136 | Common:1; Rare:78 | ||||
| chr2:677357-677768 | Common:3; Rare:139 | ||||
| chr2:1744259-1744668 | Common:3; Rare:133 | ||||
| chr2:3377791-3378039 | Common:2; Rare:72 | ||||
| chr2:3379608-3379798 | Common:2; Rare:77 | ||||
| chr2:3519449-3519674 | Common:3; Rare:66 | ||||
| chr2:3558231-3558565 | Common:6; Rare:133 | ||||
| chr2:3575120-3575350 | Common:2; Rare:67; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423169-9423697 | Common:1; Rare:147 | ||||
| chr2:9474498-9474605 | Common:6; Rare:55 | ||||
| chr2:9555621-9555893 | Common:2; Rare:85 | ||||
| chr2:9630944-9631344 | Common:3; Rare:127 | ||||
| chr2:10689898-10690024 | Common:2; Rare:49 | ||||
| chr2:11746401-11746676 | Common:2; Rare:79; Clinvar:5 | ||||
| chr2:12716675-12716987 | Common:1; Rare:94 |