Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:52038227-52038432 | Rare:79; Clinvar:10; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
chr4:52659180-52659336 | Common:1; Rare:55 | ||||
chr4:52862180-52862335 | Common:5; Rare:68 | ||||
chr4:53365997-53366222 | Rare:52 | ||||
chr4:53377493-53377912 | Common:3; Rare:138 | ||||
chr4:53558177-53558302 | Common:2; Rare:29 | ||||
chr4:54064493-54064798 | Common:4; Rare:98 | ||||
chr4:55346204-55346347 | Common:2; Rare:50; Clinvar:3; Clinvar (benign):2 | ||||
chr4:55395793-55395968 | Common:3; Rare:52; Clinvar:2 | ||||
chr4:55546489-55546746 | Common:4; Rare:52 | ||||
chr4:55546786-55547039 | Common:2; Rare:91 | ||||
chr4:55635886-55636017 | Common:2; Rare:33 | ||||
chr4:55636086-55636426 | Common:5; Rare:91 | ||||
chr4:55853501-55853778 | Rare:75 | ||||
chr4:56048914-56049289 | Common:2; Rare:103 |