| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18919344-18919744 | Common:2; Rare:141 | ||||
| chr19:18941239-18941537 | Common:4; Rare:74 | ||||
| chr19:19033467-19033649 | Common:2; Rare:60 | ||||
| chr19:19033803-19033907 | Common:1; Rare:28 | ||||
| chr19:19192122-19192258 | Common:1; Rare:41 | ||||
| chr19:19192614-19192973 | Common:2; Rare:85 | ||||
| chr19:19516167-19516331 | Rare:95; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19733073-19733254 | Common:2; Rare:46 | ||||
| chr19:19821653-19821884 | Common:1; Rare:77 | ||||
| chr19:19900763-19900991 | Common:1; Rare:67 | ||||
| chr19:20661514-20661784 | Common:7; Rare:74 | ||||
| chr19:21141900-21142094 | Rare:52 | ||||
| chr19:22784146-22784311 | Common:1; Rare:40 | ||||
| chr19:23395391-23395682 | Common:2; Rare:87 | ||||
| chr19:29213143-29213193 | Common:1; Rare:19 |