Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:86800304-86800636 | Common:2; Rare:121 | ||||
chr11:86955391-86955653 | Common:1; Rare:81 | ||||
chr11:87037773-87038080 | Common:3; Rare:138 | ||||
chr11:88337686-88337843 | Common:4; Rare:83; Clinvar:4; Clinvar (benign):3 | ||||
chr11:90222982-90223141 | Common:1; Rare:62 | ||||
chr11:93330576-93330750 | Common:2; Rare:52 | ||||
chr11:93741485-93741702 | Common:4; Rare:77 | ||||
chr11:94493789-94494024 | Common:3; Rare:67; Clinvar (benign):1 | ||||
chr11:94567322-94567368 | Common:1; Rare:14 | ||||
chr11:94973537-94973719 | Rare:52 | ||||
chr11:95067457-95067590 | Rare:54 | ||||
chr11:95089723-95089930 | Common:3; Rare:90 | ||||
chr11:95789484-95789676 | Common:1; Rare:98 | ||||
chr11:95789780-95789872 | Common:2; Rare:29 | ||||
chr11:95790318-95790565 | Rare:100 |