| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40750433-40750909 | Common:6; Rare:118 | ||||
| chr19:41353856-41354173 | Common:1; Rare:91 | ||||
| chr19:41397581-41397833 | Common:7; Rare:87; Clinvar (benign):4 | ||||
| chr19:41860080-41860305 | Common:1; Rare:92; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:41959241-41959402 | Common:1; Rare:64 | ||||
| chr19:42075791-42076226 | Common:4; Rare:122 | ||||
| chr19:42132389-42132618 | Rare:54 | ||||
| chr19:42220123-42220352 | Common:2; Rare:63 | ||||
| chr19:42242536-42242747 | Rare:64 | ||||
| chr19:42302321-42302631 | Rare:98 | ||||
| chr19:42423532-42423753 | Common:4; Rare:79 | ||||
| chr19:43596009-43596433 | Common:3; Rare:132 | ||||
| chr19:43619559-43619686 | Common:1; Rare:38 | ||||
| chr19:43670135-43670348 | Common:2; Rare:54 | ||||
| chr19:43754895-43755056 | Common:1; Rare:62 |