| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35139419-35139566 | Common:2; Rare:28 | ||||
| chr19:35139574-35139762 | Common:1; Rare:50 | ||||
| chr19:35248864-35249013 | Common:1; Rare:61 | ||||
| chr19:35545454-35545726 | Common:4; Rare:90 | ||||
| chr19:35628740-35629113 | Common:4; Rare:114 | ||||
| chr19:35648093-35648402 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35745347-35745698 | Rare:107 | ||||
| chr19:35757867-35758201 | Common:2; Rare:97 | ||||
| chr19:35900538-35900655 | Rare:27 | ||||
| chr19:35902403-35902555 | Common:1; Rare:29 | ||||
| chr19:35908181-35908390 | Common:1; Rare:66; Clinvar:2 | ||||
| chr19:36014192-36014529 | Common:2; Rare:94 | ||||
| chr19:36114796-36114978 | Common:2; Rare:77 | ||||
| chr19:36139834-36140129 | Rare:90 | ||||
| chr19:36152392-36152559 | Common:3; Rare:46 |