| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58499211-58499545 | Common:2; Rare:109; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:58519767-58520031 | Rare:70 | ||||
| chr19:58558956-58559126 | Common:1; Rare:49 | ||||
| chr19:58573282-58573637 | Common:2; Rare:89 | ||||
| chr2:677350-677598 | Common:2; Rare:101 | ||||
| chr2:1744477-1744658 | Common:2; Rare:63 | ||||
| chr2:3377811-3377920 | Rare:30 | ||||
| chr2:3379646-3379795 | Common:2; Rare:62 | ||||
| chr2:3519419-3519674 | Common:3; Rare:74 | ||||
| chr2:3558238-3558571 | Common:6; Rare:131 | ||||
| chr2:3575120-3575447 | Common:2; Rare:94; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9422306-9422355 | Rare:7 | ||||
| chr2:9422816-9422883 | Rare:8 | ||||
| chr2:9423045-9423697 | Common:2; Rare:164 | ||||
| chr2:9474498-9474642 | Common:6; Rare:70 |