Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:12764000-12764590 | Common:6; Rare:241 | ||||
chr11:12771592-12771847 | Rare:51 | ||||
chr11:16925839-16926008 | Common:4; Rare:51 | ||||
chr11:17353649-17353792 | Common:8; Rare:85 | ||||
chr11:18383380-18384090 | Common:2; Rare:142 | ||||
chr11:18384190-18384698 | Common:4; Rare:135 | ||||
chr11:27395439-27396024 | Common:4; Rare:154 | ||||
chr11:34501462-34501976 | Common:7; Rare:141 | ||||
chr11:34653940-34654260 | Rare:57 | ||||
chr11:35030710-35031210 | Common:11; Rare:116 | ||||
chr11:35082390-35082970 | Common:12; Rare:201 | ||||
chr11:35663321-35663830 | Common:1; Rare:227; Clinvar (pathogenic):2 | ||||
chr11:35927730-35928050 | Common:6; Rare:106 | ||||
chr11:36297407-36297593 | Common:1; Rare:35 | ||||
chr11:45180430-45180820 | Common:3; Rare:196 |