| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38528507-38528617 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:38618923-38619246 | Common:3; Rare:98 | ||||
| chr19:38647378-38647748 | Common:3; Rare:132 | ||||
| chr19:38723410-38723709 | Rare:83 | ||||
| chr19:38728288-38728537 | Common:1; Rare:65 | ||||
| chr19:38831721-38831943 | Common:3; Rare:89; Clinvar (benign):1 | ||||
| chr19:38849309-38849518 | Common:1; Rare:89 | ||||
| chr19:38849924-38850097 | Rare:61 | ||||
| chr19:38851268-38851410 | Rare:35 | ||||
| chr19:38852324-38852408 | Rare:19 | ||||
| chr19:38899489-38899716 | Rare:68 | ||||
| chr19:38899813-38900079 | Rare:84 | ||||
| chr19:38900122-38900195 | Rare:15 | ||||
| chr19:38930429-38930537 | Common:1; Rare:56; Clinvar (benign):1 | ||||
| chr19:38930733-38931013 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):3 |