| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18322996-18323340 | Common:3; Rare:119 | ||||
| chr19:18557688-18557905 | Common:4; Rare:56 | ||||
| chr19:18571555-18571916 | Common:5; Rare:131 | ||||
| chr19:18588693-18588838 | Rare:38 | ||||
| chr19:18683495-18683702 | Common:1; Rare:70 | ||||
| chr19:18919335-18919754 | Common:2; Rare:154 | ||||
| chr19:18941233-18941485 | Common:4; Rare:59 | ||||
| chr19:19033437-19033925 | Common:3; Rare:146 | ||||
| chr19:19192115-19192217 | Common:1; Rare:37 | ||||
| chr19:19192593-19192973 | Common:2; Rare:96 | ||||
| chr19:19320488-19320858 | Common:4; Rare:133 | ||||
| chr19:19516147-19516296 | Rare:98; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19733089-19733306 | Common:2; Rare:52 | ||||
| chr19:19821684-19821894 | Common:1; Rare:71 | ||||
| chr19:19900763-19901039 | Common:3; Rare:75 |