| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39407426-39407602 | Rare:35 | ||||
| chr19:39412856-39412917 | Common:1; Rare:7 | ||||
| chr19:39435846-39436163 | Common:6; Rare:116 | ||||
| chr19:39445436-39445849 | Common:2; Rare:123 | ||||
| chr19:39480732-39480888 | Common:3; Rare:86; Clinvar (pathogenic):1 | ||||
| chr19:39846308-39846473 | Common:1; Rare:78 | ||||
| chr19:39970924-39971214 | Common:4; Rare:81 | ||||
| chr19:39996898-39997101 | Common:5; Rare:58 | ||||
| chr19:40056130-40056270 | Rare:18 | ||||
| chr19:40056453-40056757 | Common:3; Rare:54 | ||||
| chr19:40090856-40090990 | Common:1; Rare:39 | ||||
| chr19:40285197-40285537 | Common:1; Rare:118 | ||||
| chr19:40348342-40348739 | Common:4; Rare:128 | ||||
| chr19:40366403-40366668 | Rare:74 | ||||
| chr19:40377813-40378126 | Common:2; Rare:110; Clinvar (benign):1 |