| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38899586-38899746 | Rare:42 | ||||
| chr19:38930723-38930992 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39391025-39391418 | Common:1; Rare:158 | ||||
| chr19:39406706-39406848 | Rare:53 | ||||
| chr19:39435899-39436167 | Common:5; Rare:100 | ||||
| chr19:39480725-39480912 | Common:3; Rare:103; Clinvar (pathogenic):1 | ||||
| chr19:39846312-39846473 | Common:1; Rare:75 | ||||
| chr19:39970935-39971203 | Common:4; Rare:77 | ||||
| chr19:40056192-40056253 | Rare:10 | ||||
| chr19:40285293-40285562 | Common:1; Rare:97 | ||||
| chr19:40348388-40348720 | Common:4; Rare:108 | ||||
| chr19:40444295-40444513 | Common:3; Rare:65 | ||||
| chr19:40751080-40751322 | Common:3; Rare:71 | ||||
| chr19:41219107-41219400 | Common:1; Rare:74 | ||||
| chr19:41262305-41262565 | Rare:48 |