| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48170246-48170683 | Common:2; Rare:122 | ||||
| chr19:48325480-48325598 | Common:1; Rare:25 | ||||
| chr19:48619139-48619428 | Rare:92 | ||||
| chr19:48811017-48811114 | Rare:36 | ||||
| chr19:48993304-48993510 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:48993553-48993837 | Common:2; Rare:64 | ||||
| chr19:49362367-49362497 | Rare:36 | ||||
| chr19:49451765-49451996 | Common:2; Rare:59 | ||||
| chr19:49453094-49453303 | Common:1; Rare:66 | ||||
| chr19:49665761-49666034 | Common:3; Rare:133; Clinvar (pathogenic):1 | ||||
| chr19:49712504-49712643 | Common:1; Rare:39 | ||||
| chr19:49851075-49851120 | Rare:16 | ||||
| chr19:49877319-49877531 | Rare:46 | ||||
| chr19:49929451-49929771 | Common:7; Rare:109 | ||||
| chr19:49929912-49930219 | Common:1; Rare:74 |