| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:77087548-77087565 | Common:1; Rare:4 | ||||
| chr18:79400137-79400338 | Common:2; Rare:72 | ||||
| chr18:79988256-79988671 | Common:4; Rare:134; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:572237-572618 | Common:3; Rare:186 | ||||
| chr19:574760-575060 | Common:2; Rare:82 | ||||
| chr19:633515-633724 | Common:8; Rare:100 | ||||
| chr19:893165-893484 | Common:3; Rare:133 | ||||
| chr19:984228-984374 | Common:1; Rare:54 | ||||
| chr19:1026488-1026723 | Rare:87 | ||||
| chr19:1103794-1104126 | Common:4; Rare:139 | ||||
| chr19:1132184-1132389 | Rare:85 | ||||
| chr19:1241595-1241922 | Rare:100 | ||||
| chr19:1242163-1242542 | Rare:110 | ||||
| chr19:1248313-1248584 | Common:2; Rare:79 | ||||
| chr19:1269050-1269408 | Common:2; Rare:137 |