| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9768475-9768819 | Common:5; Rare:125 | ||||
| chr19:9786078-9786193 | Rare:33 | ||||
| chr19:9793161-9793371 | Rare:42 | ||||
| chr19:9818796-9818889 | Rare:37 | ||||
| chr19:9819038-9819419 | Common:2; Rare:88 | ||||
| chr19:9827799-9827989 | Common:1; Rare:67 | ||||
| chr19:9835011-9835396 | Rare:156 | ||||
| chr19:10106586-10106730 | Common:1; Rare:54 | ||||
| chr19:10251777-10251992 | Common:1; Rare:50 | ||||
| chr19:10286872-10287042 | Common:1; Rare:54 | ||||
| chr19:10291310-10291478 | Common:1; Rare:43 | ||||
| chr19:10333508-10333715 | Rare:69 | ||||
| chr19:10353212-10353533 | Common:2; Rare:60 | ||||
| chr19:10354194-10354294 | Common:3; Rare:32; Clinvar (benign):1 | ||||
| chr19:10380487-10380800 | Common:12; Rare:93; Clinvar:5 |