Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:23321145-23321557 | Common:2; Rare:129; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr14:23321672-23321818 | Common:1; Rare:45 | ||||
chr14:23376959-23377051 | Rare:16 | ||||
chr14:23555912-23556077 | Rare:46 | ||||
chr14:23556254-23556414 | Common:1; Rare:29 | ||||
chr14:23567745-23567871 | Rare:23 | ||||
chr14:23953638-23953813 | Common:7; Rare:65 | ||||
chr14:24094061-24094365 | Common:3; Rare:78 | ||||
chr14:24094599-24094789 | Rare:42 | ||||
chr14:24114917-24115334 | Common:2; Rare:117 | ||||
chr14:24141485-24141864 | Common:2; Rare:89 | ||||
chr14:24144239-24144434 | Common:1; Rare:49 | ||||
chr14:24146564-24146682 | Rare:47 | ||||
chr14:24147229-24147504 | Common:2; Rare:72 | ||||
chr14:24195415-24195790 | Common:1; Rare:94 |