Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15305611-15305759 | Rare:32 | ||||
chr1:15758740-15758802 | Common:1; Rare:13 | ||||
chr1:16352424-16352598 | Common:3; Rare:93 | ||||
chr1:17053963-17054320 | Common:3; Rare:116; Clinvar:16; Clinvar (benign):10 | ||||
chr1:19251512-19251838 | Common:6; Rare:106 | ||||
chr1:19312113-19312333 | Common:5; Rare:97 | ||||
chr1:20661359-20661705 | Common:3; Rare:125; Clinvar:4; Clinvar (benign):6 | ||||
chr1:21290414-21290505 | Common:1; Rare:21 | ||||
chr1:21345493-21345674 | Rare:66 | ||||
chr1:23559415-23559671 | Common:2; Rare:112 | ||||
chr1:23800730-23800929 | Common:1; Rare:65 | ||||
chr1:23959627-23959854 | Common:2; Rare:61 | ||||
chr1:25232456-25232657 | Rare:79 | ||||
chr1:25247451-25247638 | Common:2; Rare:67 | ||||
chr1:25338196-25338447 | Common:1; Rare:88 |