| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49487258-49487650 | Common:10; Rare:269 | ||||
| chr19:49495976-49496476 | Common:5; Rare:307 | ||||
| chr19:49527750-49528060 | Common:7; Rare:146 | ||||
| chr19:49580516-49580736 | Common:1; Rare:112 | ||||
| chr19:49589950-49590388 | Common:5; Rare:166 | ||||
| chr19:49591058-49591236 | Common:4; Rare:57 | ||||
| chr19:49591860-49592410 | Common:4; Rare:241 | ||||
| chr19:49640085-49640532 | Common:2; Rare:252 | ||||
| chr19:49640562-49640875 | Rare:76 | ||||
| chr19:49641785-49642256 | Rare:249 | ||||
| chr19:49664372-49665356 | Common:4; Rare:309 | ||||
| chr19:49665512-49666047 | Common:9; Rare:370; Clinvar (pathogenic):2 | ||||
| chr19:49683710-49684069 | Common:4; Rare:158 | ||||
| chr19:49766484-49767018 | Common:3; Rare:176 | ||||
| chr19:49818212-49818420 | Common:6; Rare:129; Clinvar:4; Clinvar (benign):2 |