| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49496131-49496536 | Common:1; Rare:147 | ||||
| chr19:49513080-49513296 | Common:1; Rare:48 | ||||
| chr19:49527843-49528003 | Common:3; Rare:50 | ||||
| chr19:49580479-49580776 | Common:1; Rare:84 | ||||
| chr19:49589965-49590288 | Common:3; Rare:109 | ||||
| chr19:49590290-49590554 | Common:1; Rare:94 | ||||
| chr19:49591021-49591291 | Common:4; Rare:61 | ||||
| chr19:49591305-49591486 | Rare:34 | ||||
| chr19:49640119-49640830 | Common:1; Rare:171 | ||||
| chr19:49641784-49642280 | Rare:137 | ||||
| chr19:49664498-49664716 | Rare:82 | ||||
| chr19:49665345-49665481 | Rare:44 | ||||
| chr19:49665557-49665665 | Common:1; Rare:44 | ||||
| chr19:49665696-49666049 | Common:3; Rare:156; Clinvar (pathogenic):1 | ||||
| chr19:49675689-49675924 | Common:1; Rare:37 |