| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37317619-37317923 | Common:6; Rare:85 | ||||
| chr19:37370906-37371166 | Common:5; Rare:57 | ||||
| chr19:37467162-37467525 | Common:2; Rare:106 | ||||
| chr19:37594767-37594886 | Rare:29 | ||||
| chr19:37779594-37779662 | Rare:11 | ||||
| chr19:37906551-37906696 | Common:4; Rare:44 | ||||
| chr19:37907035-37907293 | Rare:59 | ||||
| chr19:38224150-38224445 | Common:1; Rare:83 | ||||
| chr19:38264765-38264889 | Rare:43 | ||||
| chr19:38315932-38316184 | Common:1; Rare:58 | ||||
| chr19:38374407-38374812 | Rare:149 | ||||
| chr19:38617922-38618283 | Common:1; Rare:71 | ||||
| chr19:38618887-38619244 | Common:4; Rare:109 | ||||
| chr19:38647404-38647733 | Common:3; Rare:120 | ||||
| chr19:38831765-38831938 | Common:3; Rare:59; Clinvar (benign):1 |