| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1026496-1026723 | Rare:84 | ||||
| chr19:1103799-1104115 | Common:4; Rare:131 | ||||
| chr19:1132109-1132455 | Common:2; Rare:136 | ||||
| chr19:1354720-1355002 | Common:2; Rare:114 | ||||
| chr19:1383437-1383571 | Common:2; Rare:78 | ||||
| chr19:1438249-1438450 | Common:1; Rare:79 | ||||
| chr19:1605397-1605665 | Common:3; Rare:104 | ||||
| chr19:2270822-2270915 | Common:4; Rare:39 | ||||
| chr19:2328550-2328703 | Common:2; Rare:74 | ||||
| chr19:2783231-2783484 | Rare:88 | ||||
| chr19:2785241-2785560 | Common:5; Rare:99 | ||||
| chr19:2841247-2841527 | Common:2; Rare:85 | ||||
| chr19:2944886-2945177 | Common:5; Rare:104 | ||||
| chr19:3761608-3761816 | Common:2; Rare:70 | ||||
| chr19:3982805-3983292 | Common:5; Rare:175; Clinvar:1; Clinvar (benign):6 |