Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:43955303-43955562 | Common:3; Rare:79 | ||||
chr22:44024164-44024351 | Common:1; Rare:64 | ||||
chr22:45163674-45164008 | Common:4; Rare:121 | ||||
chr22:46053778-46053901 | Rare:43 | ||||
chr22:46250268-46250408 | Common:1; Rare:45 | ||||
chr22:46335621-46335797 | Common:5; Rare:80; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
chr22:46762476-46762713 | Common:3; Rare:91 | ||||
chr22:50185672-50185943 | Common:5; Rare:111 | ||||
chr22:50582818-50583142 | Common:5; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
chr22:50628090-50628267 | Common:8; Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
chr22:50783592-50783882 | Common:2; Rare:95 | ||||
chr3:3126813-3126984 | Common:4; Rare:74; Clinvar (benign):1 | ||||
chr3:4303253-4303405 | Common:1; Rare:58 | ||||
chr3:4493177-4493350 | Rare:61 | ||||
chr3:8501620-8501963 | Common:2; Rare:126 |