| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10402476-10402682 | Common:1; Rare:35 | ||||
| chr19:10486697-10487026 | Rare:74 | ||||
| chr19:10653184-10653333 | Rare:44 | ||||
| chr19:10797413-10797723 | Rare:79; Clinvar (pathogenic):1 | ||||
| chr19:10959195-10959241 | Common:1; Rare:5 | ||||
| chr19:11040611-11040684 | Common:1; Rare:12 | ||||
| chr19:11068860-11068888 | Rare:5 | ||||
| chr19:11123000-11123152 | Common:2; Rare:31; Clinvar (benign):1 | ||||
| chr19:11204065-11204347 | Common:4; Rare:86 | ||||
| chr19:11210939-11211196 | Common:2; Rare:38 | ||||
| chr19:11211272-11211434 | Rare:35 | ||||
| chr19:11243144-11243370 | Common:1; Rare:82; Clinvar (pathogenic):1 | ||||
| chr19:11243377-11243633 | Common:1; Rare:84; Clinvar:1 | ||||
| chr19:11522430-11522539 | Rare:16 | ||||
| chr19:11598408-11598561 | Common:1; Rare:26 |