| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5680390-5681248 | Rare:1047 | ||||
| chr19:5686521-5686934 | Rare:211 | ||||
| chr19:5686980-5687397 | Common:6; Rare:304 | ||||
| chr19:5689852-5690416 | Common:11; Rare:495 | ||||
| chr19:5690702-5691102 | Common:2; Rare:111 | ||||
| chr19:5718878-5719790 | Common:7; Rare:537 | ||||
| chr19:5719886-5720070 | Common:1; Rare:76; Clinvar:1 | ||||
| chr19:5720003-5720443 | Common:7; Rare:711 | ||||
| chr19:5720390-5721067 | Common:18; Rare:588 | ||||
| chr19:5790128-5790994 | Common:33; Rare:727 | ||||
| chr19:5791072-5791472 | Common:40; Rare:641 | ||||
| chr19:5903661-5903955 | Common:6; Rare:355; Clinvar:15; Clinvar (benign):13 | ||||
| chr19:5903946-5904891 | Common:35; Rare:638; Clinvar:4 | ||||
| chr19:5977980-5978550 | Common:21; Rare:1040 | ||||
| chr19:6057374-6057774 | Common:2; Rare:73 |