| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35558465-35558703 | Rare:81 | ||||
| chr19:35559777-35560241 | Common:1; Rare:142 | ||||
| chr19:35560479-35560940 | Common:2; Rare:133 | ||||
| chr19:35730482-35730787 | Common:1; Rare:76; Clinvar (pathogenic):1 | ||||
| chr19:35755815-35756012 | Rare:56 | ||||
| chr19:36142646-36143125 | Rare:128 | ||||
| chr19:36150335-36150366 | Rare:7 | ||||
| chr19:36797283-36797543 | Rare:56 | ||||
| chr19:38691960-38692334 | Common:3; Rare:74 | ||||
| chr19:38714373-38714576 | Common:1; Rare:61; Clinvar (benign):1 | ||||
| chr19:38845718-38845912 | Common:1; Rare:64 | ||||
| chr19:39376259-39376507 | Rare:46 | ||||
| chr19:39389723-39390045 | Rare:67 | ||||
| chr19:39392416-39392518 | Rare:32 | ||||
| chr19:39402658-39402946 | Rare:76 |