| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18539410-18539663 | Common:4; Rare:83 | ||||
| chr19:18557680-18557892 | Common:5; Rare:55 | ||||
| chr19:18571678-18571891 | Common:2; Rare:92 | ||||
| chr19:18919335-18919763 | Common:3; Rare:161 | ||||
| chr19:19033482-19033653 | Common:2; Rare:52 | ||||
| chr19:19033805-19033920 | Common:1; Rare:33 | ||||
| chr19:19192110-19192268 | Common:1; Rare:50 | ||||
| chr19:19192624-19192973 | Common:2; Rare:83 | ||||
| chr19:19320480-19320858 | Common:4; Rare:138 | ||||
| chr19:19516145-19516331 | Rare:117; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19821682-19821905 | Common:1; Rare:75 | ||||
| chr19:21329279-21329504 | Common:2; Rare:48 | ||||
| chr19:22634106-22634346 | Common:7; Rare:68 | ||||
| chr19:29213114-29213213 | Common:1; Rare:36 | ||||
| chr19:29606186-29606320 | Rare:44 |