| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49157678-49157835 | Rare:45; Clinvar:1 | ||||
| chr19:49362380-49362473 | Rare:26 | ||||
| chr19:49451748-49452002 | Common:3; Rare:66 | ||||
| chr19:49453024-49453311 | Common:2; Rare:88 | ||||
| chr19:49487335-49487675 | Common:5; Rare:134 | ||||
| chr19:49580536-49580648 | Rare:38 | ||||
| chr19:49581241-49581418 | Common:1; Rare:35 | ||||
| chr19:49641826-49641977 | Rare:44 | ||||
| chr19:49665756-49666029 | Common:3; Rare:134; Clinvar (pathogenic):1 | ||||
| chr19:49867526-49867632 | Common:2; Rare:37; Clinvar:1 | ||||
| chr19:49877299-49877717 | Common:1; Rare:106 | ||||
| chr19:49877839-49878161 | Common:4; Rare:101 | ||||
| chr19:49929430-49929820 | Common:7; Rare:132 | ||||
| chr19:49929923-49930219 | Common:1; Rare:70 | ||||
| chr19:50476240-50476542 | Rare:140 |