| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34926831-34926918 | Common:1; Rare:36 | ||||
| chr19:35154651-35154851 | Rare:35 | ||||
| chr19:35155117-35155230 | Rare:22 | ||||
| chr19:35319022-35319392 | Common:3; Rare:61 | ||||
| chr19:35545446-35545698 | Common:4; Rare:82 | ||||
| chr19:35612653-35612792 | Common:1; Rare:49 | ||||
| chr19:35628720-35629094 | Common:4; Rare:111 | ||||
| chr19:35648113-35648402 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35745381-35745698 | Rare:93 | ||||
| chr19:35748286-35748604 | Common:3; Rare:91 | ||||
| chr19:35757867-35758213 | Common:2; Rare:104 | ||||
| chr19:35899726-35899871 | Common:1; Rare:47 | ||||
| chr19:35900524-35900623 | Rare:20 | ||||
| chr19:36014192-36014570 | Common:2; Rare:106 | ||||
| chr19:36054390-36054572 | Common:3; Rare:52 |