| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11559167-11559459 | Common:4; Rare:86 | ||||
| chr19:11597305-11597512 | Common:1; Rare:63 | ||||
| chr19:11924961-11925134 | Common:6; Rare:48 | ||||
| chr19:12156710-12156852 | Common:1; Rare:33 | ||||
| chr19:12401237-12401350 | Rare:30 | ||||
| chr19:12551430-12551726 | Common:2; Rare:82 | ||||
| chr19:12610792-12610994 | Rare:74 | ||||
| chr19:12666639-12666830 | Rare:82; Clinvar:4 | ||||
| chr19:12669007-12669146 | Common:1; Rare:36 | ||||
| chr19:12681047-12681547 | Common:2; Rare:160 | ||||
| chr19:12681553-12681906 | Common:3; Rare:185; Clinvar (pathogenic):1 | ||||
| chr19:12696520-12696690 | Rare:73 | ||||
| chr19:12721967-12722418 | Common:1; Rare:78 | ||||
| chr19:12722519-12722843 | Common:4; Rare:65 | ||||
| chr19:12723783-12724037 | Common:1; Rare:67 |