| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40716865-40716957 | Rare:26 | ||||
| chr19:40750441-40750909 | Common:6; Rare:117 | ||||
| chr19:40798891-40799242 | Common:6; Rare:128 | ||||
| chr19:41310133-41310268 | Rare:53 | ||||
| chr19:41363801-41363977 | Common:1; Rare:62; Clinvar:1 | ||||
| chr19:41364123-41364343 | Rare:67; Clinvar:1 | ||||
| chr19:41397305-41397604 | Common:5; Rare:85 | ||||
| chr19:41860129-41860278 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:42075872-42076193 | Rare:84 | ||||
| chr19:42220128-42220303 | Common:1; Rare:43 | ||||
| chr19:42302421-42302478 | Rare:14 | ||||
| chr19:42325394-42325663 | Rare:69 | ||||
| chr19:43527176-43527310 | Common:4; Rare:53; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr19:43553472-43553616 | Rare:39 | ||||
| chr19:43575468-43575743 | Common:1; Rare:83 |