| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44141410-44141649 | Common:3; Rare:33 | ||||
| chr19:44304992-44305141 | Rare:41 | ||||
| chr19:44356645-44356851 | Common:1; Rare:43 | ||||
| chr19:44500483-44500632 | Common:1; Rare:44 | ||||
| chr19:44643801-44643937 | Rare:37 | ||||
| chr19:44757363-44757569 | Rare:52; Clinvar:1 | ||||
| chr19:44954924-44955017 | Common:2; Rare:26 | ||||
| chr19:44955251-44955404 | Common:2; Rare:43 | ||||
| chr19:45091591-45091818 | Common:1; Rare:58 | ||||
| chr19:45406339-45406659 | Common:1; Rare:74 | ||||
| chr19:45423502-45423676 | Common:2; Rare:35; Clinvar (benign):1 | ||||
| chr19:45450738-45451023 | Common:4; Rare:53 | ||||
| chr19:45468494-45468529 | Rare:2 | ||||
| chr19:45496945-45497271 | Common:2; Rare:97 | ||||
| chr19:45507404-45507768 | Rare:104 |