Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25232452-25232741 | Common:1; Rare:102 | ||||
chr1:25246527-25246749 | Rare:102 | ||||
chr1:25247108-25247202 | Rare:31 | ||||
chr1:25247271-25247748 | Common:6; Rare:159 | ||||
chr1:25338098-25338528 | Common:2; Rare:134 | ||||
chr1:25338782-25338923 | Common:1; Rare:31 | ||||
chr1:25429905-25429979 | Rare:12 | ||||
chr1:25430068-25430453 | Common:6; Rare:111 | ||||
chr1:25430869-25431062 | Common:1; Rare:74 | ||||
chr1:25431077-25431506 | Common:2; Rare:134 | ||||
chr1:25543558-25543719 | Rare:72; Clinvar:5 | ||||
chr1:25799874-25799940 | Common:1; Rare:12 | ||||
chr1:25800048-25800246 | Rare:76; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:25800383-25800463 | Rare:14; Clinvar:1; Clinvar (benign):1 | ||||
chr1:25819686-25820236 | Common:6; Rare:155 |