Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:144082513-144082674 | Common:2; Rare:57 | ||||
chr8:144084573-144084873 | Common:2; Rare:107 | ||||
chr8:144096437-144096741 | Common:1; Rare:112; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr8:144104175-144104510 | Common:3; Rare:107 | ||||
chr8:144106623-144106958 | Common:3; Rare:107 | ||||
chr8:144137657-144137818 | Common:1; Rare:47 | ||||
chr8:144291328-144291618 | Common:1; Rare:94 | ||||
chr8:144508996-144509106 | Rare:33 | ||||
chr8:144509822-144509958 | Rare:59 | ||||
chr8:144517748-144518029 | Common:1; Rare:99; Clinvar:7; Clinvar (benign):1 | ||||
chr8:144792335-144792561 | Common:3; Rare:85 | ||||
chr8:144827241-144827608 | Common:2; Rare:95 | ||||
chr8:144901451-144901755 | Common:1; Rare:82 | ||||
chr8:145052809-145053124 | Common:1; Rare:100 | ||||
chr9:2844045-2844382 | Common:7; Rare:132 |