| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9435503-9435622 | Rare:47 | ||||
| chr19:9538579-9538716 | Common:1; Rare:37 | ||||
| chr19:9584465-9584596 | Common:1; Rare:46 | ||||
| chr19:9621192-9621542 | Common:3; Rare:97 | ||||
| chr19:9675015-9675130 | Common:1; Rare:26 | ||||
| chr19:9768588-9768814 | Common:3; Rare:77 | ||||
| chr19:9786114-9786219 | Rare:31 | ||||
| chr19:9818809-9818887 | Rare:32 | ||||
| chr19:9827808-9827982 | Common:1; Rare:67 | ||||
| chr19:9835013-9835376 | Rare:152 | ||||
| chr19:10106301-10106387 | Rare:40 | ||||
| chr19:10315743-10316044 | Common:7; Rare:137; Clinvar (benign):12 | ||||
| chr19:10333512-10333738 | Rare:74 | ||||
| chr19:10380487-10380839 | Common:13; Rare:106; Clinvar:5 | ||||
| chr19:10403424-10403929 | Rare:169 |