| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44072047-44072164 | Common:1; Rare:30 | ||||
| chr19:44141410-44141643 | Common:3; Rare:32 | ||||
| chr19:44304992-44305145 | Rare:43 | ||||
| chr19:44356681-44356838 | Common:1; Rare:30 | ||||
| chr19:45038941-45039094 | Rare:52 | ||||
| chr19:45322819-45322911 | Rare:18 | ||||
| chr19:45322924-45323132 | Common:2; Rare:41 | ||||
| chr19:45406363-45406680 | Common:2; Rare:78 | ||||
| chr19:45507228-45507523 | Common:1; Rare:79 | ||||
| chr19:46296838-46297076 | Common:4; Rare:90 | ||||
| chr19:46298120-46298456 | Common:5; Rare:80 | ||||
| chr19:46346941-46347115 | Common:3; Rare:54 | ||||
| chr19:46600913-46601414 | Common:5; Rare:173; Clinvar (benign):1 | ||||
| chr19:47256472-47256583 | Rare:42 | ||||
| chr19:47484261-47484318 | Rare:14 |