| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49580534-49580664 | Rare:43 | ||||
| chr19:49665813-49665980 | Common:2; Rare:85; Clinvar (pathogenic):1 | ||||
| chr19:49851058-49851154 | Rare:37 | ||||
| chr19:49877277-49877726 | Common:1; Rare:117 | ||||
| chr19:50476370-50476550 | Rare:84 | ||||
| chr19:50511142-50511304 | Rare:57 | ||||
| chr19:51751858-51752022 | Common:2; Rare:38 | ||||
| chr19:51927332-51927487 | Common:1; Rare:44 | ||||
| chr19:52008166-52008359 | Rare:58 | ||||
| chr19:52028336-52028433 | Common:2; Rare:24 | ||||
| chr19:52048641-52048697 | Rare:10 | ||||
| chr19:52397733-52397880 | Common:2; Rare:44 | ||||
| chr19:52527469-52527703 | Common:3; Rare:85 | ||||
| chr19:52735024-52735178 | Common:4; Rare:42 | ||||
| chr19:53254795-53255057 | Common:4; Rare:96 |