| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:2328552-2328703 | Common:2; Rare:72 | ||||
| chr19:2783243-2783431 | Rare:69 | ||||
| chr19:2785356-2785544 | Common:2; Rare:57 | ||||
| chr19:4007480-4007758 | Common:3; Rare:104 | ||||
| chr19:4182524-4182713 | Common:1; Rare:68 | ||||
| chr19:4246940-4247113 | Common:2; Rare:57 | ||||
| chr19:4867658-4867859 | Common:2; Rare:58 | ||||
| chr19:5622737-5623150 | Common:5; Rare:155 | ||||
| chr19:5978078-5978415 | Common:3; Rare:130 | ||||
| chr19:7395022-7395188 | Common:4; Rare:52 | ||||
| chr19:7489028-7489103 | Rare:32 | ||||
| chr19:7534054-7534188 | Common:3; Rare:35; Clinvar (benign):1 | ||||
| chr19:7535407-7535750 | Common:3; Rare:102; Clinvar:2 | ||||
| chr19:7629529-7629848 | Common:5; Rare:115; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7637002-7637152 | Common:2; Rare:48; Clinvar (benign):1 |