| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50025160-50025212 | Rare:8 | ||||
| chr19:50025274-50025730 | Common:7; Rare:156 | ||||
| chr19:50025867-50026152 | Common:1; Rare:75 | ||||
| chr19:50203440-50203705 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:50203979-50204060 | Rare:11 | ||||
| chr19:50328981-50329415 | Common:2; Rare:118; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:50329460-50329682 | Common:1; Rare:47 | ||||
| chr19:50333142-50333320 | Common:1; Rare:47 | ||||
| chr19:50333334-50333546 | Common:1; Rare:47 | ||||
| chr19:50333576-50333688 | Common:2; Rare:19 | ||||
| chr19:50333857-50334026 | Common:2; Rare:83 | ||||
| chr19:50376234-50376559 | Common:6; Rare:82 | ||||
| chr19:50376710-50376847 | Common:1; Rare:34 | ||||
| chr19:50383936-50384434 | Common:4; Rare:199; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:50384506-50384758 | Rare:56 |