| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:782450-782780 | Rare:87 | ||||
| chr19:860568-860724 | Rare:63; Clinvar (pathogenic):1 | ||||
| chr19:940851-941351 | Common:25; Rare:324 | ||||
| chr19:1027482-1027801 | Common:4; Rare:58 | ||||
| chr19:1028137-1028533 | Common:5; Rare:82 | ||||
| chr19:1028637-1028792 | Rare:38 | ||||
| chr19:1074838-1075036 | Common:3; Rare:88 | ||||
| chr19:1101721-1102028 | Common:4; Rare:60 | ||||
| chr19:1102513-1102661 | Common:2; Rare:42 | ||||
| chr19:1172829-1173176 | Common:2; Rare:82 | ||||
| chr19:1180587-1180787 | Rare:48 | ||||
| chr19:1181766-1181905 | Rare:32 | ||||
| chr19:1183950-1184124 | Common:3; Rare:42 | ||||
| chr19:1189502-1189670 | Common:1; Rare:33 | ||||
| chr19:1194518-1194728 | Common:4; Rare:61 |