Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:76782086-76782366 | Common:1; Rare:34 | ||||
chr11:76783029-76783379 | Common:10; Rare:117 | ||||
chr11:76997980-76998190 | Rare:34 | ||||
chr11:77034269-77034478 | Rare:35 | ||||
chr11:77066796-77067045 | Common:1; Rare:82 | ||||
chr11:77473541-77473841 | Common:1; Rare:102 | ||||
chr11:77589872-77589987 | Rare:34 | ||||
chr11:77637588-77637860 | Common:1; Rare:90 | ||||
chr11:77820862-77821210 | Common:1; Rare:102 | ||||
chr11:77994822-77995040 | Rare:53 | ||||
chr11:78079803-78079942 | Common:2; Rare:46 | ||||
chr11:78139590-78139779 | Common:3; Rare:76; Clinvar:2 | ||||
chr11:78188592-78188925 | Common:2; Rare:106 | ||||
chr11:78417739-78418023 | Common:2; Rare:116 | ||||
chr11:78574761-78574970 | Common:2; Rare:85; Clinvar (benign):1 |