| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11355177-11355513 | Common:1; Rare:96 | ||||
| chr19:11374521-11374744 | Common:1; Rare:75 | ||||
| chr19:11374851-11375254 | Common:2; Rare:131 | ||||
| chr19:11380934-11381143 | Rare:67; Clinvar (benign):1 | ||||
| chr19:11381166-11381631 | Common:2; Rare:129; Clinvar:1 | ||||
| chr19:11381688-11382057 | Common:1; Rare:136; Clinvar (benign):3 | ||||
| chr19:11382837-11383019 | Common:1; Rare:65 | ||||
| chr19:11384255-11384498 | Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:11418463-11418801 | Common:1; Rare:99 | ||||
| chr19:11419276-11419465 | Common:1; Rare:39 | ||||
| chr19:11435094-11435299 | Common:2; Rare:54 | ||||
| chr19:11435522-11435770 | Common:4; Rare:94; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:11436054-11436198 | Rare:57 | ||||
| chr19:11505112-11505490 | Common:1; Rare:143 | ||||
| chr19:11505708-11506021 | Common:2; Rare:134 |