Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:45163804-45164008 | Common:2; Rare:73 | ||||
chr22:45413571-45413734 | Rare:66 | ||||
chr22:46053778-46053863 | Rare:31 | ||||
chr22:46250268-46250408 | Common:1; Rare:45 | ||||
chr22:46296745-46296922 | Rare:59 | ||||
chr22:46335621-46335804 | Common:5; Rare:83; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
chr22:46762496-46762693 | Common:3; Rare:74 | ||||
chr22:50185664-50185938 | Common:5; Rare:106 | ||||
chr22:50244986-50245133 | Common:1; Rare:58 | ||||
chr22:50582784-50583136 | Common:7; Rare:114; Clinvar:2; Clinvar (benign):3 | ||||
chr22:50783628-50783853 | Common:1; Rare:65 | ||||
chr3:3126775-3126984 | Common:4; Rare:90; Clinvar (benign):1 | ||||
chr3:4303253-4303362 | Common:1; Rare:35 | ||||
chr3:8501644-8501931 | Common:2; Rare:105 | ||||
chr3:9362976-9363117 | Common:1; Rare:53 |