| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40777934-40778298 | Common:1; Rare:102 | ||||
| chr19:41218863-41219417 | Common:4; Rare:133 | ||||
| chr19:41310086-41310279 | Rare:76 | ||||
| chr19:41364069-41364160 | Common:1; Rare:27; Clinvar:4 | ||||
| chr19:41364165-41364328 | Rare:50 | ||||
| chr19:41397310-41397584 | Common:5; Rare:74 | ||||
| chr19:41860121-41860524 | Common:5; Rare:152; Clinvar:4; Clinvar (benign):2 | ||||
| chr19:41860977-41861209 | Rare:75; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:41959272-41959456 | Common:1; Rare:61 | ||||
| chr19:42075817-42076168 | Rare:91 | ||||
| chr19:42220128-42220347 | Common:2; Rare:62 | ||||
| chr19:42302428-42302503 | Rare:14 | ||||
| chr19:43527147-43527276 | Common:5; Rare:60; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43575459-43575753 | Common:1; Rare:89 | ||||
| chr19:43580483-43580643 | Common:3; Rare:25 |