| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35134620-35134716 | Rare:32 | ||||
| chr19:35138613-35138883 | Rare:67 | ||||
| chr19:35139346-35139631 | Common:3; Rare:62 | ||||
| chr19:35142940-35143306 | Rare:87 | ||||
| chr19:35154226-35154527 | Rare:49 | ||||
| chr19:35155155-35155230 | Rare:15 | ||||
| chr19:35248885-35249025 | Common:1; Rare:62 | ||||
| chr19:35268976-35269140 | Common:1; Rare:21 | ||||
| chr19:35291976-35292193 | Common:2; Rare:46 | ||||
| chr19:35545446-35545725 | Common:4; Rare:91 | ||||
| chr19:35628872-35629103 | Common:3; Rare:70 | ||||
| chr19:35648107-35648402 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35745397-35745710 | Rare:91 | ||||
| chr19:35748283-35748612 | Common:3; Rare:92 | ||||
| chr19:35757939-35758204 | Common:2; Rare:79 |