Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:30559106-30559216 | Common:1; Rare:42 | ||||
chr14:31025207-31025668 | Common:2; Rare:107 | ||||
chr14:31207607-31207926 | Common:2; Rare:106 | ||||
chr14:31208146-31208180 | Rare:6 | ||||
chr14:31420525-31420763 | Common:3; Rare:71 | ||||
chr14:31457350-31457577 | Common:2; Rare:80 | ||||
chr14:31561353-31561450 | Common:1; Rare:37; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:32075987-32076127 | Common:2; Rare:30 | ||||
chr14:32076251-32076312 | Rare:17 | ||||
chr14:32076651-32077045 | Common:3; Rare:117 | ||||
chr14:32329211-32329382 | Rare:27 | ||||
chr14:32934464-32934504 | Rare:12 | ||||
chr14:33951070-33951249 | Common:1; Rare:59 | ||||
chr14:34018736-34018834 | Rare:14 | ||||
chr14:34228098-34228333 | Common:3; Rare:38 |