Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:77473564-77473782 | Common:1; Rare:83 | ||||
chr11:77637733-77637868 | Common:1; Rare:51 | ||||
chr11:77820698-77821210 | Common:2; Rare:149 | ||||
chr11:78139581-78139809 | Common:3; Rare:91; Clinvar:2 | ||||
chr11:78188592-78188933 | Common:2; Rare:109 | ||||
chr11:78574832-78574966 | Common:1; Rare:44 | ||||
chr11:83071795-83072124 | Common:4; Rare:91 | ||||
chr11:83156682-83156796 | Rare:38 | ||||
chr11:83193640-83193765 | Common:1; Rare:56 | ||||
chr11:83285898-83286087 | Common:3; Rare:81 | ||||
chr11:83682223-83682533 | Common:1; Rare:52 | ||||
chr11:85628333-85628652 | Common:7; Rare:108 | ||||
chr11:85647882-85648033 | Common:1; Rare:38; Clinvar:2; Clinvar (benign):1 | ||||
chr11:86244457-86244786 | Common:1; Rare:84 | ||||
chr11:87037762-87038040 | Common:3; Rare:132 |