| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49487272-49487644 | Common:5; Rare:131 | ||||
| chr19:49496276-49496471 | Common:1; Rare:74 | ||||
| chr19:49580534-49580648 | Rare:38 | ||||
| chr19:49665813-49666020 | Common:2; Rare:109; Clinvar (pathogenic):1 | ||||
| chr19:49690973-49691150 | Common:2; Rare:40 | ||||
| chr19:49813161-49813341 | Rare:72 | ||||
| chr19:49850613-49851027 | Common:1; Rare:126 | ||||
| chr19:49867212-49867397 | Common:2; Rare:63; Clinvar (benign):3 | ||||
| chr19:49877319-49877717 | Common:1; Rare:99 | ||||
| chr19:49929430-49929820 | Common:7; Rare:132 | ||||
| chr19:49929971-49930223 | Common:1; Rare:59 | ||||
| chr19:50025325-50025725 | Common:7; Rare:133 | ||||
| chr19:50384028-50384377 | Common:2; Rare:147; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:50476234-50476556 | Common:1; Rare:149 | ||||
| chr19:50511142-50511273 | Rare:46 |