Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38831781-38832050 | Common:3; Rare:74 | ||||
chr19:38899531-38900026 | Rare:150 | ||||
chr19:38930722-38930996 | Common:3; Rare:79; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39391054-39391419 | Common:1; Rare:151 | ||||
chr19:39406618-39406848 | Common:1; Rare:63 | ||||
chr19:39435841-39436163 | Common:6; Rare:117 | ||||
chr19:39445480-39445752 | Common:2; Rare:75 | ||||
chr19:39970938-39971214 | Common:4; Rare:77 | ||||
chr19:40348381-40348751 | Common:4; Rare:122 | ||||
chr19:40715076-40715145 | Rare:22 | ||||
chr19:40716880-40717146 | Common:1; Rare:83 | ||||
chr19:41264981-41265109 | Common:2; Rare:27 | ||||
chr19:41353582-41353627 | Rare:8 | ||||
chr19:41397332-41397589 | Common:4; Rare:64 | ||||
chr19:42302318-42302473 | Rare:50 |