Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:23057502-23057673 | Common:2; Rare:41 | ||||
chr14:23071254-23071465 | Rare:73 | ||||
chr14:23094521-23094728 | Common:2; Rare:72 | ||||
chr14:23094975-23095594 | Common:3; Rare:247 | ||||
chr14:23321519-23321813 | Common:2; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
chr14:23555955-23556389 | Common:4; Rare:105 | ||||
chr14:23567756-23567978 | Rare:47 | ||||
chr14:23953639-23953813 | Common:7; Rare:64 | ||||
chr14:24114962-24115292 | Common:2; Rare:97 | ||||
chr14:24146568-24146913 | Common:1; Rare:108 | ||||
chr14:24147238-24147547 | Common:2; Rare:89 | ||||
chr14:24192429-24192656 | Common:2; Rare:49 | ||||
chr14:24195412-24195748 | Common:1; Rare:76 | ||||
chr14:24213052-24213182 | Rare:22 | ||||
chr14:24215951-24216059 | Common:1; Rare:42 |