Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68332880-68333300 | Common:3; Rare:147 | ||||
chr10:68406953-68407073 | Common:1; Rare:37 | ||||
chr10:68407181-68407400 | Common:8; Rare:136 | ||||
chr10:68471869-68472042 | Common:2; Rare:168; Clinvar (benign):3 | ||||
chr10:68527293-68527651 | Common:6; Rare:206 | ||||
chr10:68721018-68721291 | Common:3; Rare:143 | ||||
chr10:68721484-68721738 | Common:1; Rare:82 | ||||
chr10:68827010-68827280 | Common:3; Rare:117 | ||||
chr10:68827409-68827537 | Common:1; Rare:53 | ||||
chr10:68901049-68901370 | Common:5; Rare:183 | ||||
chr10:68956050-68956491 | Common:4; Rare:212 | ||||
chr10:68988729-68988855 | Common:1; Rare:42; Clinvar (benign):2 | ||||
chr10:69179905-69180352 | Common:6; Rare:290 | ||||
chr10:69318683-69318916 | Common:7; Rare:130 | ||||
chr10:69408680-69409010 | Common:18; Rare:99 |