| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18919352-18919726 | Common:2; Rare:122 | ||||
| chr19:19033482-19033653 | Common:2; Rare:52 | ||||
| chr19:19192128-19192344 | Common:2; Rare:60; Clinvar (benign):1 | ||||
| chr19:19516157-19516241 | Rare:43 | ||||
| chr19:19821708-19821905 | Common:1; Rare:65 | ||||
| chr19:19865714-19865940 | Common:2; Rare:60 | ||||
| chr19:19900758-19900953 | Rare:55 | ||||
| chr19:20167177-20167214 | Rare:17 | ||||
| chr19:20923114-20923264 | Rare:37 | ||||
| chr19:21020517-21020704 | Common:3; Rare:38 | ||||
| chr19:21082049-21082215 | Rare:31 | ||||
| chr19:32971939-32972239 | Common:4; Rare:83 | ||||
| chr19:34677581-34677762 | Common:4; Rare:53 | ||||
| chr19:35138481-35138795 | Common:1; Rare:61 | ||||
| chr19:35139583-35139648 | Rare:16 |