| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48965038-48965359 | Common:1; Rare:83; Clinvar (pathogenic):4 | ||||
| chr19:48965468-48965609 | Rare:45; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:48993241-48993541 | Common:3; Rare:136; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:48993552-48993930 | Common:5; Rare:98 | ||||
| chr19:49084892-49085604 | Common:3; Rare:238 | ||||
| chr19:49114271-49114424 | Common:1; Rare:39 | ||||
| chr19:49128119-49128268 | Common:2; Rare:45 | ||||
| chr19:49155388-49155609 | Rare:39 | ||||
| chr19:49157689-49157843 | Rare:45; Clinvar:1 | ||||
| chr19:49310038-49310296 | Rare:74 | ||||
| chr19:49334930-49335193 | Common:2; Rare:41 | ||||
| chr19:49335397-49335458 | Common:1; Rare:13 | ||||
| chr19:49360416-49360627 | Common:1; Rare:44 | ||||
| chr19:49361515-49361619 | Rare:21 | ||||
| chr19:49362380-49362483 | Rare:30 |