Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:94493800-94494029 | Common:3; Rare:66; Clinvar (benign):1 | ||||
chr11:94973528-94973733 | Rare:62 | ||||
chr11:95067452-95067588 | Rare:54 | ||||
chr11:95089725-95090014 | Common:3; Rare:110 | ||||
chr11:95789430-95789564 | Common:1; Rare:64 | ||||
chr11:95789569-95789890 | Common:3; Rare:143 | ||||
chr11:95790351-95790592 | Common:1; Rare:94 | ||||
chr11:95923776-95923860 | Rare:21 | ||||
chr11:95923944-95924133 | Common:1; Rare:83; Clinvar (benign):2 | ||||
chr11:96389856-96390043 | Common:1; Rare:76 | ||||
chr11:100687142-100687315 | Common:2; Rare:48 | ||||
chr11:101914869-101915073 | Common:4; Rare:58 | ||||
chr11:101915106-101915362 | Common:3; Rare:74 | ||||
chr11:102110203-102110470 | Common:1; Rare:103 | ||||
chr11:102317333-102317521 | Rare:43 |