Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25859359-25859580 | Common:3; Rare:93 | ||||
chr1:25906397-25906590 | Rare:75 | ||||
chr1:26111737-26111874 | Rare:44 | ||||
chr1:26279928-26280203 | Rare:147 | ||||
chr1:26306600-26306835 | Common:9; Rare:61 | ||||
chr1:26432123-26432468 | Common:4; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26442513-26442766 | Common:3; Rare:50 | ||||
chr1:26472143-26472627 | Common:5; Rare:163 | ||||
chr1:26545533-26545892 | Common:1; Rare:72 | ||||
chr1:26787859-26788237 | Common:3; Rare:111; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890211-26890336 | Common:1; Rare:48 | ||||
chr1:26900017-26900221 | Rare:81 | ||||
chr1:26900441-26900555 | Rare:38 | ||||
chr1:26921529-26921926 | Common:3; Rare:123 | ||||
chr1:26945384-26945697 | Rare:85 |