| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:47190263-47190459 | Common:1; Rare:34 | ||||
| chr19:47226094-47226274 | Rare:57 | ||||
| chr19:47229582-47229651 | Rare:7 | ||||
| chr19:47229673-47229823 | Rare:26 | ||||
| chr19:47243108-47243456 | Common:4; Rare:79 | ||||
| chr19:47264658-47264899 | Common:1; Rare:115 | ||||
| chr19:47328771-47328848 | Common:2; Rare:12 | ||||
| chr19:47482628-47482835 | Common:2; Rare:33 | ||||
| chr19:47490700-47490822 | Rare:41 | ||||
| chr19:47513725-47513749 | Rare:14 | ||||
| chr19:47600320-47600641 | Rare:80 | ||||
| chr19:47640384-47640527 | Common:1; Rare:22 | ||||
| chr19:47757035-47757204 | Common:4; Rare:64 | ||||
| chr19:48061599-48061671 | Common:2; Rare:11 | ||||
| chr19:48119136-48119276 | Common:2; Rare:31; Clinvar (benign):1 |