Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:42893022-42893356 | Common:4; Rare:121 | ||||
chr21:43659465-43659592 | Common:1; Rare:43 | ||||
chr21:44299961-44300123 | Common:1; Rare:62; Clinvar (benign):1 | ||||
chr21:44873631-44874021 | Common:8; Rare:158 | ||||
chr21:44939913-44940060 | Common:2; Rare:43 | ||||
chr21:45287831-45288118 | Common:6; Rare:112 | ||||
chr21:45404885-45405227 | Common:13; Rare:190 | ||||
chr21:45981514-45981840 | Common:23; Rare:79; Clinvar (benign):2 | ||||
chr21:45987505-45987646 | Rare:66; Clinvar:8; Clinvar (benign):4 | ||||
chr21:46098625-46098791 | Common:2; Rare:39 | ||||
chr21:46184413-46184689 | Common:3; Rare:26 | ||||
chr21:46286230-46286408 | Common:4; Rare:67 | ||||
chr21:46323830-46324193 | Common:2; Rare:123; Clinvar:1; Clinvar (benign):1 | ||||
chr21:46458711-46459063 | Common:3; Rare:121 | ||||
chr22:17159233-17159357 | Common:4; Rare:60 |