| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18636719-18637057 | Common:2; Rare:84 | ||||
| chr19:18683467-18683705 | Common:2; Rare:75 | ||||
| chr19:18683851-18683960 | Rare:31 | ||||
| chr19:18919341-18919768 | Common:3; Rare:157 | ||||
| chr19:18941077-18941449 | Common:6; Rare:107 | ||||
| chr19:19033436-19033649 | Common:2; Rare:73 | ||||
| chr19:19033798-19033952 | Common:1; Rare:38 | ||||
| chr19:19033984-19034143 | Common:1; Rare:34 | ||||
| chr19:19192096-19192328 | Common:1; Rare:68 | ||||
| chr19:19192563-19192976 | Common:2; Rare:108 | ||||
| chr19:19203395-19203585 | Rare:62 | ||||
| chr19:19211994-19212028 | Rare:5 | ||||
| chr19:19320476-19320862 | Common:4; Rare:142 | ||||
| chr19:19464484-19464704 | Common:1; Rare:36 | ||||
| chr19:19516147-19516306 | Rare:102; Clinvar:1; Clinvar (pathogenic):1 |