| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:55141301-55141461 | Common:3; Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:55146433-55146656 | Common:2; Rare:81; Clinvar (benign):1 | ||||
| chr19:55146681-55147055 | Common:5; Rare:122; Clinvar:1; Clinvar (benign):5 | ||||
| chr19:55147490-55147713 | Common:7; Rare:29 | ||||
| chr19:55156221-55156539 | Common:3; Rare:108; Clinvar:13; Clinvar (benign):7 | ||||
| chr19:55160624-55160861 | Common:1; Rare:115; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:55166558-55166826 | Common:2; Rare:100; Clinvar:5; Clinvar (benign):4 | ||||
| chr19:55175037-55175268 | Common:5; Rare:83 | ||||
| chr19:55207239-55207356 | Common:1; Rare:42 | ||||
| chr19:55239407-55239674 | Common:1; Rare:95 | ||||
| chr19:55258906-55259165 | Common:1; Rare:95 | ||||
| chr19:55280166-55280526 | Rare:86 | ||||
| chr19:55283754-55284104 | Common:1; Rare:77 | ||||
| chr19:55339601-55339948 | Common:1; Rare:92 | ||||
| chr19:55341317-55341495 | Common:1; Rare:37 |