| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42220024-42220581 | Common:3; Rare:148 | ||||
| chr19:42242511-42242966 | Common:1; Rare:157 | ||||
| chr19:42243084-42243394 | Common:3; Rare:111 | ||||
| chr19:42250353-42250508 | Rare:34; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:42253604-42253964 | Common:4; Rare:119 | ||||
| chr19:42254344-42254544 | Common:1; Rare:63 | ||||
| chr19:42255058-42255290 | Common:1; Rare:84 | ||||
| chr19:42268192-42268616 | Rare:88 | ||||
| chr19:42268620-42269024 | Rare:95 | ||||
| chr19:42269039-42269301 | Rare:66 | ||||
| chr19:42279868-42280096 | Common:2; Rare:45 | ||||
| chr19:42280238-42280271 | Rare:5 | ||||
| chr19:42280321-42280644 | Common:1; Rare:72 | ||||
| chr19:42283700-42284149 | Rare:142 | ||||
| chr19:42284211-42284333 | Common:1; Rare:33 |