| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5293213-5293433 | Common:1; Rare:99 | ||||
| chr19:5622717-5623203 | Common:5; Rare:194 | ||||
| chr19:5680685-5681034 | Rare:84 | ||||
| chr19:5791148-5791343 | Common:5; Rare:60 | ||||
| chr19:5978078-5978393 | Common:3; Rare:117 | ||||
| chr19:6110467-6110834 | Common:2; Rare:110 | ||||
| chr19:6464075-6464340 | Common:1; Rare:50 | ||||
| chr19:6739529-6739769 | Common:6; Rare:66 | ||||
| chr19:7394991-7395195 | Common:6; Rare:65 | ||||
| chr19:7488993-7489103 | Rare:50 | ||||
| chr19:7535543-7535787 | Common:3; Rare:89; Clinvar:2 | ||||
| chr19:7629531-7629854 | Common:5; Rare:115; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636985-7637152 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr19:7888390-7888547 | Common:1; Rare:35 | ||||
| chr19:7943644-7943990 | Rare:90 |