Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24555999-24556149 | Common:2; Rare:44 | ||||
chr1:25232448-25232648 | Rare:80 | ||||
chr1:25246932-25247125 | Rare:72 | ||||
chr1:25247307-25247630 | Common:3; Rare:122 | ||||
chr1:25338238-25338447 | Common:1; Rare:73 | ||||
chr1:25819878-25820029 | Common:3; Rare:47 | ||||
chr1:25859370-25859531 | Common:2; Rare:65 | ||||
chr1:26111714-26111851 | Common:1; Rare:50 | ||||
chr1:26280019-26280185 | Rare:96 | ||||
chr1:26432156-26432403 | Common:4; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472237-26472627 | Common:4; Rare:142 | ||||
chr1:26695721-26696032 | Common:1; Rare:103 | ||||
chr1:26787877-26788243 | Common:3; Rare:104; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26889831-26889926 | Rare:31 | ||||
chr1:26890229-26890344 | Common:1; Rare:46 |