Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:74732545-74732807 | Common:4; Rare:60 | ||||
chr1:74732994-74733324 | Common:6; Rare:114 | ||||
chr1:74733326-74733493 | Rare:61 | ||||
chr1:74733601-74733645 | Common:1; Rare:4 | ||||
chr1:74733720-74733926 | Common:1; Rare:29 | ||||
chr1:75724038-75724100 | Common:1; Rare:12 | ||||
chr1:75724231-75724470 | Common:4; Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
chr1:75724501-75725033 | Common:6; Rare:183; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:75785734-75785999 | Rare:59 | ||||
chr1:75786019-75786374 | Common:5; Rare:134 | ||||
chr1:75786696-75786766 | Common:1; Rare:20 | ||||
chr1:75787748-75788001 | Rare:66 | ||||
chr1:75791152-75791259 | Rare:22 | ||||
chr1:76074512-76074761 | Common:2; Rare:100 | ||||
chr1:77218968-77219009 | Common:1; Rare:6 |