| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50804499-50804991 | Common:28; Rare:405 | ||||
| chr19:50804952-50805494 | Common:7; Rare:147 | ||||
| chr19:50968502-50969170 | Common:12; Rare:216 | ||||
| chr19:51001133-51001257 | Common:2; Rare:34 | ||||
| chr19:51001530-51002410 | Common:8; Rare:295 | ||||
| chr19:51016973-51017141 | Rare:46 | ||||
| chr19:51019699-51019816 | Common:3; Rare:27 | ||||
| chr19:51020000-51020420 | Common:14; Rare:81 | ||||
| chr19:51026543-51026759 | Common:3; Rare:91 | ||||
| chr19:51034725-51035163 | Common:5; Rare:114 | ||||
| chr19:51108293-51108647 | Common:4; Rare:198 | ||||
| chr19:51339701-51340059 | Common:2; Rare:135 | ||||
| chr19:51366303-51366815 | Common:21; Rare:297; Clinvar (benign):6 | ||||
| chr19:51366820-51366984 | Common:1; Rare:32 | ||||
| chr19:51367486-51367987 | Common:8; Rare:388 |