| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18683486-18683699 | Common:1; Rare:72 | ||||
| chr19:18919344-18919726 | Common:2; Rare:128 | ||||
| chr19:19033475-19033653 | Common:2; Rare:55 | ||||
| chr19:19033803-19033916 | Common:1; Rare:30 | ||||
| chr19:19192110-19192239 | Common:1; Rare:40 | ||||
| chr19:19192624-19192972 | Common:2; Rare:83 | ||||
| chr19:19320464-19320857 | Common:4; Rare:150 | ||||
| chr19:19516161-19516302 | Rare:84; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19821660-19821878 | Common:1; Rare:73 | ||||
| chr19:19900795-19900986 | Common:1; Rare:47 | ||||
| chr19:20565731-20565959 | Rare:65 | ||||
| chr19:20661487-20661755 | Common:7; Rare:79 | ||||
| chr19:21851983-21852219 | Common:1; Rare:63 | ||||
| chr19:22052375-22052513 | Common:1; Rare:19 | ||||
| chr19:22532392-22532702 | Common:3; Rare:82 |