| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:54115271-54115455 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr19:54115630-54115787 | Common:1; Rare:35; Clinvar:4 | ||||
| chr19:54159659-54160073 | Rare:141 | ||||
| chr19:54189349-54189421 | Common:1; Rare:25 | ||||
| chr19:54191196-54191285 | Common:1; Rare:30 | ||||
| chr19:54200705-54200891 | Common:2; Rare:72 | ||||
| chr19:54449030-54449285 | Common:3; Rare:80 | ||||
| chr19:54449412-54449516 | Rare:34 | ||||
| chr19:55242244-55242496 | Rare:96 | ||||
| chr19:55258987-55259150 | Common:1; Rare:52 | ||||
| chr19:55385717-55385965 | Common:5; Rare:85 | ||||
| chr19:55461675-55461979 | Common:4; Rare:82 | ||||
| chr19:55599500-55599547 | Rare:20 | ||||
| chr19:55624568-55624717 | Common:2; Rare:64 | ||||
| chr19:55643435-55643651 | Common:3; Rare:67 |