| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58059164-58059294 | Rare:71 | ||||
| chr19:58098200-58098474 | Common:8; Rare:102 | ||||
| chr19:58183315-58183449 | Rare:46 | ||||
| chr19:58228859-58228946 | Rare:29 | ||||
| chr19:58278664-58278991 | Common:3; Rare:100 | ||||
| chr19:58326864-58327029 | Common:1; Rare:35 | ||||
| chr19:58347546-58347777 | Common:8; Rare:103 | ||||
| chr19:58401227-58401568 | Common:6; Rare:107 | ||||
| chr19:58440134-58440448 | Common:6; Rare:82 | ||||
| chr19:58451483-58451629 | Common:1; Rare:52 | ||||
| chr19:58499211-58499625 | Common:2; Rare:142; Clinvar:6; Clinvar (benign):1 | ||||
| chr19:58519786-58520054 | Rare:77 | ||||
| chr19:58558952-58559196 | Common:1; Rare:74 | ||||
| chr19:58573468-58573595 | Common:1; Rare:34 | ||||
| chr2:677341-677557 | Common:1; Rare:93 |