Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:19033467-19033653 | Common:2; Rare:61 | ||||
chr19:19034002-19034108 | Common:1; Rare:23 | ||||
chr19:19192124-19192200 | Common:1; Rare:27 | ||||
chr19:19211818-19212000 | Rare:52 | ||||
chr19:19320480-19320871 | Common:4; Rare:143 | ||||
chr19:19516163-19516259 | Rare:49; Clinvar (pathogenic):1 | ||||
chr19:19733053-19733207 | Common:1; Rare:39 | ||||
chr19:19821668-19821839 | Common:1; Rare:62 | ||||
chr19:19865681-19865945 | Common:2; Rare:75 | ||||
chr19:19900795-19900975 | Common:1; Rare:43 | ||||
chr19:20167054-20167238 | Common:1; Rare:67 | ||||
chr19:20661519-20661784 | Common:7; Rare:72 | ||||
chr19:21020485-21020674 | Rare:37 | ||||
chr19:21836170-21836331 | Rare:64 | ||||
chr19:22634092-22634358 | Common:7; Rare:78 |