Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24143120-24143302 | Rare:46 | ||||
chr1:24187258-24187441 | Common:2; Rare:48 | ||||
chr1:24642890-24643329 | Common:2; Rare:146 | ||||
chr1:25232442-25232657 | Rare:87 | ||||
chr1:25247076-25247136 | Rare:14 | ||||
chr1:25247419-25247638 | Common:2; Rare:84 | ||||
chr1:25338163-25338447 | Common:1; Rare:99 | ||||
chr1:25819878-25820029 | Common:3; Rare:47 | ||||
chr1:26279923-26280162 | Rare:135 | ||||
chr1:26432112-26432426 | Common:4; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472293-26472532 | Common:4; Rare:78 | ||||
chr1:26473047-26473286 | Rare:125 | ||||
chr1:26787859-26788234 | Common:3; Rare:111; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890248-26890336 | Common:1; Rare:34 | ||||
chr1:26900411-26900524 | Rare:46 |