| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42423501-42423813 | Common:4; Rare:107 | ||||
| chr19:43504073-43504355 | Common:6; Rare:92 | ||||
| chr19:43504690-43504902 | Common:2; Rare:48 | ||||
| chr19:43525593-43525692 | Rare:9 | ||||
| chr19:43527155-43527346 | Common:5; Rare:71; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43532636-43532723 | Common:1; Rare:17 | ||||
| chr19:43532767-43532991 | Common:1; Rare:44 | ||||
| chr19:43533054-43533580 | Common:3; Rare:155 | ||||
| chr19:43575417-43575928 | Common:3; Rare:130 | ||||
| chr19:43580420-43580607 | Common:4; Rare:33 | ||||
| chr19:43595225-43595345 | Rare:37 | ||||
| chr19:43596043-43596659 | Common:3; Rare:187 | ||||
| chr19:43618969-43619194 | Rare:47 | ||||
| chr19:43619219-43619570 | Rare:83 | ||||
| chr19:43619575-43619761 | Common:3; Rare:59 |