Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:93784185-93784399 | Common:3; Rare:61 | ||||
chr11:94128802-94129131 | Common:3; Rare:108 | ||||
chr11:94129409-94129455 | Rare:15 | ||||
chr11:94493780-94494053 | Common:5; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
chr11:94973508-94973719 | Rare:69 | ||||
chr11:95067459-95067573 | Rare:40 | ||||
chr11:95089695-95089930 | Common:3; Rare:105 | ||||
chr11:95231406-95231587 | Common:2; Rare:46 | ||||
chr11:95789478-95789872 | Common:4; Rare:182 | ||||
chr11:95790359-95790598 | Common:1; Rare:91 | ||||
chr11:95923829-95924164 | Common:2; Rare:147; Clinvar:5; Clinvar (benign):5 | ||||
chr11:96343128-96343366 | Common:2; Rare:64 | ||||
chr11:96389842-96390076 | Common:2; Rare:96 | ||||
chr11:101127324-101127850 | Common:6; Rare:214 | ||||
chr11:101128970-101129178 | Common:5; Rare:62 |