| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34677376-34677729 | Common:7; Rare:96 | ||||
| chr19:34733956-34734260 | Common:2; Rare:87 | ||||
| chr19:34734467-34734566 | Rare:24 | ||||
| chr19:35013657-35013858 | Common:2; Rare:46 | ||||
| chr19:35154659-35154968 | Rare:53 | ||||
| chr19:35155333-35155608 | Rare:75 | ||||
| chr19:35248633-35248761 | Rare:37 | ||||
| chr19:35268431-35268578 | Rare:26 | ||||
| chr19:35328959-35329235 | Common:1; Rare:65 | ||||
| chr19:35331729-35331754 | Rare:6 | ||||
| chr19:35344833-35345125 | Common:2; Rare:97 | ||||
| chr19:35545493-35545716 | Common:4; Rare:71 | ||||
| chr19:35612612-35612797 | Common:2; Rare:64 | ||||
| chr19:35628837-35629102 | Common:4; Rare:81 | ||||
| chr19:35648077-35648398 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 |