| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:52048632-52048687 | Rare:9 | ||||
| chr19:52171448-52171546 | Common:1; Rare:23 | ||||
| chr19:52397750-52397894 | Common:4; Rare:46 | ||||
| chr19:52690478-52690638 | Common:4; Rare:36 | ||||
| chr19:52735005-52735167 | Common:3; Rare:46 | ||||
| chr19:52962791-52963052 | Common:4; Rare:82 | ||||
| chr19:53103351-53103782 | Common:3; Rare:125 | ||||
| chr19:53254833-53255023 | Common:1; Rare:60 | ||||
| chr19:53554454-53554547 | Common:1; Rare:31 | ||||
| chr19:53554677-53554827 | Rare:38 | ||||
| chr19:53866341-53866384 | Common:1; Rare:9 | ||||
| chr19:53867583-53867943 | Common:1; Rare:88 | ||||
| chr19:54102673-54102891 | Common:3; Rare:57 | ||||
| chr19:54115271-54115455 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr19:54115628-54115787 | Common:1; Rare:38; Clinvar:4 |