Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24745051-24745622 | Common:5; Rare:198 | ||||
chr1:25232442-25232650 | Rare:84 | ||||
chr1:25338180-25338440 | Common:1; Rare:93 | ||||
chr1:25819897-25820013 | Common:2; Rare:35 | ||||
chr1:25859400-25859558 | Common:1; Rare:55 | ||||
chr1:26279910-26280162 | Rare:142 | ||||
chr1:26306614-26306837 | Common:10; Rare:57 | ||||
chr1:26432057-26432415 | Common:5; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472180-26472539 | Common:4; Rare:116 | ||||
chr1:26787877-26788199 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26900435-26900476 | Rare:14 | ||||
chr1:26921491-26921815 | Common:3; Rare:93 | ||||
chr1:27322123-27322332 | Common:1; Rare:88 | ||||
chr1:27725693-27725998 | Common:2; Rare:89 | ||||
chr1:27772980-27773276 | Common:1; Rare:100 |