Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:119018292-119018808 | Common:13; Rare:197 | ||||
chr11:119057048-119057419 | Common:3; Rare:136 | ||||
chr11:119067632-119067838 | Common:3; Rare:69 | ||||
chr11:119101788-119101895 | Rare:32; Clinvar:1 | ||||
chr11:119121279-119121626 | Common:1; Rare:79 | ||||
chr11:119206211-119206325 | Common:4; Rare:51; Clinvar:6; Clinvar (benign):4 | ||||
chr11:119317097-119317281 | Rare:61 | ||||
chr11:120128833-120129069 | Common:1; Rare:48 | ||||
chr11:120336709-120336719 | Rare:2 | ||||
chr11:121292586-121292798 | Rare:73; Clinvar:3 | ||||
chr11:122882845-122882943 | Rare:26 | ||||
chr11:123062064-123062328 | Common:5; Rare:112 | ||||
chr11:123062352-123062666 | Common:4; Rare:144 | ||||
chr11:123741649-123741751 | Rare:19 | ||||
chr11:124673712-124673940 | Common:4; Rare:67 |