| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18281383-18281482 | Rare:34 | ||||
| chr19:18919328-18919783 | Common:3; Rare:178 | ||||
| chr19:19033515-19033610 | Common:1; Rare:33 | ||||
| chr19:19192107-19192269 | Common:1; Rare:50 | ||||
| chr19:19192599-19193032 | Common:3; Rare:103; Clinvar (benign):1 | ||||
| chr19:19320480-19320852 | Common:4; Rare:134 | ||||
| chr19:19516145-19516247 | Rare:60 | ||||
| chr19:20661578-20661675 | Common:4; Rare:19 | ||||
| chr19:29213094-29213232 | Common:2; Rare:50 | ||||
| chr19:29606187-29606321 | Rare:44 | ||||
| chr19:29665252-29665569 | Common:4; Rare:107 | ||||
| chr19:31349227-31349512 | Common:4; Rare:96 | ||||
| chr19:32692250-32692390 | Common:2; Rare:77 | ||||
| chr19:32971889-32972208 | Common:3; Rare:95 | ||||
| chr19:34399760-34399960 | Rare:61; Clinvar (pathogenic):1 |