Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20661343-20661727 | Common:3; Rare:137; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20787228-20787511 | Rare:137 | ||||
chr1:21345477-21345655 | Common:1; Rare:69 | ||||
chr1:21783048-21783279 | Common:2; Rare:81 | ||||
chr1:23344233-23344585 | Common:2; Rare:114 | ||||
chr1:23559467-23559648 | Common:1; Rare:76 | ||||
chr1:23691595-23691867 | Common:4; Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
chr1:23778281-23778515 | Common:9; Rare:120 | ||||
chr1:23791075-23791221 | Rare:44 | ||||
chr1:23800732-23800959 | Common:1; Rare:80 | ||||
chr1:23825421-23825565 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
chr1:23959603-23959854 | Common:2; Rare:67 | ||||
chr1:24413723-24413896 | Common:1; Rare:34 | ||||
chr1:24642971-24643327 | Common:2; Rare:112 | ||||
chr1:25232454-25232657 | Rare:80 |