| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:54448466-54448670 | Rare:30 | ||||
| chr19:54448845-54448877 | Rare:7 | ||||
| chr19:54448996-54449594 | Common:12; Rare:192 | ||||
| chr19:54463590-54463861 | Common:1; Rare:68 | ||||
| chr19:54463955-54464220 | Common:5; Rare:69 | ||||
| chr19:54473096-54473220 | Common:1; Rare:21 | ||||
| chr19:54473231-54473571 | Common:1; Rare:78 | ||||
| chr19:54966271-54966414 | Common:3; Rare:43 | ||||
| chr19:55063058-55063177 | Common:7; Rare:58 | ||||
| chr19:55080163-55080456 | Common:2; Rare:89 | ||||
| chr19:55080664-55080703 | Common:1; Rare:8 | ||||
| chr19:55087065-55087362 | Common:1; Rare:105 | ||||
| chr19:55117513-55117987 | Common:8; Rare:132 | ||||
| chr19:55141291-55141474 | Common:3; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:55166276-55166296 | Rare:8 |