| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17859521-17860004 | Common:4; Rare:141 | ||||
| chr19:17860117-17860188 | Common:1; Rare:20 | ||||
| chr19:17932655-17933124 | Common:2; Rare:136 | ||||
| chr19:17933276-17933312 | Rare:7 | ||||
| chr19:17950826-17950993 | Common:1; Rare:36 | ||||
| chr19:17951203-17951351 | Rare:26 | ||||
| chr19:17951835-17952323 | Common:4; Rare:124 | ||||
| chr19:17966914-17967152 | Rare:64 | ||||
| chr19:18000716-18000820 | Rare:26 | ||||
| chr19:18000972-18001158 | Common:1; Rare:37 | ||||
| chr19:18001247-18001481 | Rare:59 | ||||
| chr19:18007975-18008236 | Common:5; Rare:92 | ||||
| chr19:18152392-18152793 | Common:1; Rare:104 | ||||
| chr19:18152877-18153309 | Common:2; Rare:127 | ||||
| chr19:18161332-18161614 | Common:2; Rare:73; Clinvar (benign):2 |