| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49813142-49813350 | Rare:83 | ||||
| chr19:49818221-49818344 | Common:4; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:49850463-49850735 | Rare:67 | ||||
| chr19:49851045-49851182 | Common:1; Rare:55 | ||||
| chr19:49857663-49857976 | Common:2; Rare:140 | ||||
| chr19:49866995-49867496 | Common:4; Rare:171; Clinvar:7; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr19:49867534-49867658 | Common:2; Rare:37 | ||||
| chr19:49877251-49877742 | Common:2; Rare:126 | ||||
| chr19:49929404-49929594 | Common:4; Rare:67 | ||||
| chr19:49929884-49930273 | Common:2; Rare:98 | ||||
| chr19:50025322-50025702 | Common:7; Rare:126 | ||||
| chr19:50329476-50329696 | Common:1; Rare:51 | ||||
| chr19:50333523-50333606 | Common:2; Rare:15 | ||||
| chr19:50333644-50333950 | Common:4; Rare:101 | ||||
| chr19:50384028-50384384 | Common:2; Rare:150; Clinvar:1; Clinvar (benign):2 |