Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70354994-70355098 | Rare:40 | ||||
chr1:70410762-70410829 | Rare:12 | ||||
chr1:70411029-70411331 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080952-71081436 | Rare:135 | ||||
chr1:74198064-74198453 | Common:3; Rare:180 | ||||
chr1:74733000-74733245 | Common:5; Rare:75 | ||||
chr1:74733282-74733458 | Rare:72 | ||||
chr1:75724237-75725047 | Common:10; Rare:267; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr1:75786059-75786420 | Common:5; Rare:129 | ||||
chr1:76074552-76074699 | Common:2; Rare:56 | ||||
chr1:77219281-77219552 | Common:1; Rare:118 | ||||
chr1:77682555-77682732 | Rare:43 | ||||
chr1:77682924-77683165 | Common:2; Rare:51 | ||||
chr1:77683195-77683719 | Common:2; Rare:146 | ||||
chr1:77759228-77759321 | Rare:20 |