| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11381601-11381860 | Rare:109; Clinvar (benign):3 | ||||
| chr19:11435089-11435276 | Common:2; Rare:47 | ||||
| chr19:11435512-11435700 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:11505078-11505499 | Common:2; Rare:157 | ||||
| chr19:11505549-11506062 | Common:2; Rare:184 | ||||
| chr19:11528822-11528956 | Rare:31 | ||||
| chr19:11529057-11529336 | Common:1; Rare:50 | ||||
| chr19:11554157-11554421 | Rare:85 | ||||
| chr19:11559101-11559514 | Common:4; Rare:110 | ||||
| chr19:11578592-11578692 | Rare:21 | ||||
| chr19:11578892-11579121 | Common:1; Rare:47 | ||||
| chr19:11597283-11597570 | Common:2; Rare:82 | ||||
| chr19:11738850-11739185 | Common:4; Rare:92 | ||||
| chr19:11766827-11767353 | Common:2; Rare:127 | ||||
| chr19:11798395-11798613 | Common:2; Rare:49 |