Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:93721277-93721542 | Common:2; Rare:72 | ||||
chr11:93740027-93740177 | Common:1; Rare:28 | ||||
chr11:94129722-94129868 | Common:1; Rare:35 | ||||
chr11:94183731-94184023 | Common:6; Rare:66 | ||||
chr11:94184090-94184518 | Rare:82 | ||||
chr11:94184614-94184878 | Common:1; Rare:44 | ||||
chr11:94459502-94459752 | Rare:49; Clinvar:3; Clinvar (benign):3 | ||||
chr11:94794732-94795160 | Common:2; Rare:95 | ||||
chr11:94810387-94810667 | Common:5; Rare:45 | ||||
chr11:94812168-94812349 | Common:1; Rare:37 | ||||
chr11:95068469-95068760 | Rare:42 | ||||
chr11:95825001-95825129 | Rare:27 | ||||
chr11:95857578-95857833 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
chr11:95877053-95877253 | Rare:36 | ||||
chr11:96057713-96057737 | Rare:3 |