| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48965710-48965857 | Common:1; Rare:57; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:48993296-48993915 | Common:7; Rare:202; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:49085100-49085505 | Common:3; Rare:163 | ||||
| chr19:49451754-49452022 | Common:3; Rare:75 | ||||
| chr19:49487282-49487644 | Common:5; Rare:130 | ||||
| chr19:49580528-49580609 | Rare:28 | ||||
| chr19:49665778-49666044 | Common:2; Rare:133; Clinvar (pathogenic):1 | ||||
| chr19:49877319-49877717 | Common:1; Rare:99 | ||||
| chr19:49877905-49878157 | Common:2; Rare:80 | ||||
| chr19:49929451-49929838 | Common:7; Rare:134 | ||||
| chr19:49929923-49930219 | Common:1; Rare:70 | ||||
| chr19:50476255-50476539 | Rare:132 | ||||
| chr19:52028351-52028462 | Common:2; Rare:20 | ||||
| chr19:52397750-52397879 | Common:2; Rare:38 | ||||
| chr19:52962861-52963109 | Common:3; Rare:76 |