| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50567244-50567955 | Common:3; Rare:190 | ||||
| chr19:50568210-50568670 | Rare:77 | ||||
| chr19:50639697-50640118 | Common:11; Rare:211 | ||||
| chr19:50658066-50658438 | Common:1; Rare:97 | ||||
| chr19:50803990-50804291 | Common:5; Rare:94 | ||||
| chr19:50804922-50805149 | Common:4; Rare:58 | ||||
| chr19:51108315-51108671 | Common:2; Rare:87 | ||||
| chr19:51339724-51340025 | Common:1; Rare:64 | ||||
| chr19:51366285-51366632 | Common:8; Rare:105; Clinvar (benign):2 | ||||
| chr19:51367495-51367927 | Common:4; Rare:136 | ||||
| chr19:51571128-51571342 | Common:4; Rare:66 | ||||
| chr19:51887770-51888240 | Rare:125 | ||||
| chr19:51904934-51905107 | Common:3; Rare:53 | ||||
| chr19:51927280-51927502 | Common:1; Rare:72 | ||||
| chr19:51986788-51987032 | Common:2; Rare:68 |