| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18153007-18153280 | Common:1; Rare:91 | ||||
| chr19:18571632-18571891 | Common:3; Rare:103 | ||||
| chr19:18919335-18919738 | Common:2; Rare:144 | ||||
| chr19:19033482-19033632 | Common:2; Rare:47 | ||||
| chr19:19033814-19033916 | Common:1; Rare:27 | ||||
| chr19:19192124-19192262 | Common:1; Rare:43 | ||||
| chr19:19192614-19192991 | Common:2; Rare:89 | ||||
| chr19:19320480-19320811 | Common:4; Rare:109 | ||||
| chr19:19516167-19516277 | Rare:63; Clinvar (pathogenic):1 | ||||
| chr19:19900795-19900971 | Common:1; Rare:42 | ||||
| chr19:21836174-21836310 | Rare:54 | ||||
| chr19:32405916-32406138 | Common:2; Rare:73 | ||||
| chr19:32971932-32972284 | Common:4; Rare:99 | ||||
| chr19:34172351-34172551 | Rare:86 | ||||
| chr19:34254525-34254602 | Rare:20 |