| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:57599758-57599920 | Common:2; Rare:49 | ||||
| chr19:57727608-57727810 | Common:1; Rare:55 | ||||
| chr19:57814885-57815018 | Rare:35 | ||||
| chr19:58002773-58002973 | Common:2; Rare:94 | ||||
| chr19:58059205-58059301 | Rare:54 | ||||
| chr19:58098200-58098474 | Common:8; Rare:102 | ||||
| chr19:58155071-58155195 | Common:1; Rare:34 | ||||
| chr19:58183311-58183454 | Rare:49 | ||||
| chr19:58278611-58278991 | Common:3; Rare:115 | ||||
| chr19:58326875-58327064 | Common:1; Rare:45 | ||||
| chr19:58327231-58327336 | Rare:25 | ||||
| chr19:58347568-58347773 | Common:7; Rare:97 | ||||
| chr19:58408458-58408686 | Common:3; Rare:69 | ||||
| chr19:58440134-58440460 | Common:6; Rare:88 | ||||
| chr19:58499211-58499646 | Common:2; Rare:154; Clinvar:6; Clinvar (benign):1 |