Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:15029661-15029968 | Common:1; Rare:45 | ||||
chr16:15715162-15715406 | Common:1; Rare:65; Clinvar:4; Clinvar (benign):8 | ||||
chr16:15719222-15719538 | Common:1; Rare:98; Clinvar:6; Clinvar (benign):3 | ||||
chr16:15720280-15720468 | Common:1; Rare:50; Clinvar:3; Clinvar (benign):4 | ||||
chr16:15727132-15727181 | Rare:14 | ||||
chr16:15735522-15735814 | Common:4; Rare:74; Clinvar:5; Clinvar (benign):3 | ||||
chr16:15747872-15748045 | Common:4; Rare:52; Clinvar:2; Clinvar (benign):4 | ||||
chr16:15854911-15855152 | Common:2; Rare:51 | ||||
chr16:17266995-17267105 | Common:1; Rare:20 | ||||
chr16:19393692-19394011 | Common:1; Rare:79 | ||||
chr16:21501544-21501750 | Rare:29 | ||||
chr16:21501888-21502323 | Common:3; Rare:94 | ||||
chr16:21519900-21520023 | Common:1; Rare:42 | ||||
chr16:21820380-21820484 | Rare:27 | ||||
chr16:22195794-22195925 | Common:4; Rare:64 |