Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27211775-27212109 | Common:3; Rare:117 | ||||
chr2:27212223-27212443 | Common:2; Rare:118 | ||||
chr2:27217115-27217546 | Common:1; Rare:148 | ||||
chr2:27263038-27263213 | Rare:44 | ||||
chr2:27282321-27282501 | Rare:27 | ||||
chr2:27322540-27322731 | Rare:44 | ||||
chr2:27323043-27323154 | Rare:27; Clinvar (benign):1 | ||||
chr2:27356738-27356855 | Rare:30 | ||||
chr2:27356961-27357199 | Common:2; Rare:87 | ||||
chr2:27370257-27370648 | Common:1; Rare:160 | ||||
chr2:27371074-27371328 | Common:1; Rare:75 | ||||
chr2:27380553-27380856 | Common:2; Rare:120; Clinvar:6 | ||||
chr2:27429016-27429135 | Common:1; Rare:39 | ||||
chr2:27442215-27442403 | Common:1; Rare:59 | ||||
chr2:27489643-27489838 | Rare:53; Clinvar (benign):1 |