Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24745244-24745578 | Common:2; Rare:114 | ||||
chr1:24745587-24745613 | Rare:6 | ||||
chr1:25232444-25232657 | Rare:86 | ||||
chr1:25246986-25247125 | Rare:43 | ||||
chr1:25338180-25338447 | Common:1; Rare:95 | ||||
chr1:25819878-25820029 | Common:3; Rare:47 | ||||
chr1:25859370-25859580 | Common:2; Rare:85 | ||||
chr1:26279926-26280162 | Rare:132 | ||||
chr1:26339207-26339264 | Rare:10 | ||||
chr1:26432199-26432433 | Common:4; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472128-26472420 | Common:5; Rare:82 | ||||
chr1:26862974-26863621 | Rare:175 | ||||
chr1:26863625-26863728 | Rare:28 | ||||
chr1:26921522-26921837 | Common:3; Rare:98 | ||||
chr1:26960361-26960525 | Common:1; Rare:33 |