| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7488997-7489059 | Rare:29 | ||||
| chr19:7522396-7522647 | Common:2; Rare:82 | ||||
| chr19:7535504-7535769 | Common:3; Rare:94; Clinvar:2 | ||||
| chr19:7561077-7561239 | Common:3; Rare:42; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:7629523-7629848 | Common:5; Rare:117; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7633688-7633961 | Common:4; Rare:48 | ||||
| chr19:7636973-7637176 | Common:2; Rare:60; Clinvar (benign):1 | ||||
| chr19:7888405-7888523 | Common:1; Rare:29 | ||||
| chr19:7903779-7903935 | Rare:60 | ||||
| chr19:7910765-7911025 | Common:1; Rare:116 | ||||
| chr19:7920276-7920364 | Rare:40 | ||||
| chr19:7943644-7943990 | Rare:90 | ||||
| chr19:8321324-8321703 | Common:2; Rare:153 | ||||
| chr19:8390038-8390449 | Common:2; Rare:115 | ||||
| chr19:8444807-8445052 | Common:2; Rare:114 |