Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:64427116-64427457 | Common:1; Rare:67 | ||||
chr14:65032388-65032640 | Common:1; Rare:55 | ||||
chr14:65046986-65047267 | Common:1; Rare:37 | ||||
chr14:65064847-65064969 | Rare:20 | ||||
chr14:65065528-65065681 | Rare:33 | ||||
chr14:65468382-65468556 | Common:4; Rare:33 | ||||
chr14:67724923-67725202 | Common:2; Rare:78; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr14:67729127-67729233 | Rare:30; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr14:68547643-68547803 | Common:1; Rare:17 | ||||
chr14:68565212-68565274 | Rare:5 | ||||
chr14:68628385-68628447 | Rare:18 | ||||
chr14:68937897-68938071 | Common:2; Rare:34 | ||||
chr14:75258958-75259415 | Common:2; Rare:108 | ||||
chr14:75269278-75269446 | Rare:36 | ||||
chr14:75277024-75277321 | Common:1; Rare:66 |