| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:663111-663482 | Common:3; Rare:149 | ||||
| chr19:750889-751168 | Common:2; Rare:66 | ||||
| chr19:798750-798807 | Common:1; Rare:21 | ||||
| chr19:893135-893484 | Common:3; Rare:148 | ||||
| chr19:913153-913274 | Rare:39 | ||||
| chr19:984266-984368 | Rare:36 | ||||
| chr19:1013064-1013264 | Common:2; Rare:63 | ||||
| chr19:1021196-1021545 | Common:14; Rare:152 | ||||
| chr19:1026488-1026664 | Rare:71 | ||||
| chr19:1067063-1067331 | Common:2; Rare:80 | ||||
| chr19:1103794-1104115 | Common:4; Rare:135 | ||||
| chr19:1105180-1105460 | Common:1; Rare:125; Clinvar (pathogenic):1 | ||||
| chr19:1174254-1174548 | Common:2; Rare:95 | ||||
| chr19:1251526-1251892 | Common:1; Rare:156 | ||||
| chr19:1253265-1253528 | Common:5; Rare:103 |