| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18571626-18571919 | Common:8; Rare:236 | ||||
| chr19:18588694-18588883 | Rare:51 | ||||
| chr19:18636735-18637061 | Common:3; Rare:137 | ||||
| chr19:18683434-18683694 | Common:3; Rare:137 | ||||
| chr19:18831798-18832109 | Common:2; Rare:215 | ||||
| chr19:18919341-18919774 | Common:5; Rare:305 | ||||
| chr19:18939930-18940410 | Common:2; Rare:152 | ||||
| chr19:18940390-18940750 | Common:2; Rare:150 | ||||
| chr19:18941143-18941430 | Common:4; Rare:82 | ||||
| chr19:19033434-19033765 | Common:4; Rare:200 | ||||
| chr19:19033805-19033941 | Common:1; Rare:35 | ||||
| chr19:19105670-19105880 | Common:1; Rare:114; Clinvar (pathogenic):2 | ||||
| chr19:19120998-19122051 | Common:7; Rare:441 | ||||
| chr19:19138431-19138615 | Common:2; Rare:52 | ||||
| chr19:19192084-19192282 | Common:2; Rare:111 |