Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:73876791-73877004 | Common:4; Rare:56 | ||||
chr11:74170974-74171380 | Common:3; Rare:131 | ||||
chr11:74949086-74949283 | Common:6; Rare:48 | ||||
chr11:76444663-76444919 | Rare:58 | ||||
chr11:77637739-77637843 | Common:1; Rare:44 | ||||
chr11:78139602-78139779 | Common:3; Rare:69 | ||||
chr11:88337721-88337872 | Common:3; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
chr11:93741493-93741690 | Common:4; Rare:71 | ||||
chr11:94493802-94493984 | Common:3; Rare:54; Clinvar (benign):1 | ||||
chr11:103092090-103092339 | Common:3; Rare:97 | ||||
chr11:106077554-106077682 | Common:1; Rare:46 | ||||
chr11:111912657-111912806 | Common:1; Rare:33 | ||||
chr11:111913138-111913294 | Rare:45 | ||||
chr11:112086723-112086899 | Rare:72 | ||||
chr11:112226238-112226472 | Rare:89 |