| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48965247-48965832 | Common:1; Rare:198; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48993247-48993518 | Common:2; Rare:121; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:48993553-48993912 | Common:5; Rare:94 | ||||
| chr19:49085126-49085604 | Common:3; Rare:187 | ||||
| chr19:49085606-49085629 | Rare:6 | ||||
| chr19:49128454-49128609 | Rare:46 | ||||
| chr19:49361498-49361702 | Rare:37 | ||||
| chr19:49362380-49362477 | Rare:30 | ||||
| chr19:49447022-49447486 | Common:5; Rare:149 | ||||
| chr19:49451735-49452002 | Common:3; Rare:70 | ||||
| chr19:49453092-49453317 | Common:1; Rare:71 | ||||
| chr19:49453446-49453583 | Rare:47 | ||||
| chr19:49495966-49496273 | Common:2; Rare:97 | ||||
| chr19:49580526-49580670 | Rare:49 | ||||
| chr19:49591430-49591709 | Common:9; Rare:78 |