Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:207370-207526 | Common:4; Rare:62 | ||||
chr11:208615-208854 | Rare:86 | ||||
chr11:236331-236559 | Common:8; Rare:74 | ||||
chr11:236834-237052 | Common:2; Rare:80 | ||||
chr11:307955-308250 | Common:14; Rare:70 | ||||
chr11:314774-315043 | Common:3; Rare:77 | ||||
chr11:417303-417520 | Rare:50 | ||||
chr11:560701-561016 | Common:6; Rare:146 | ||||
chr11:576413-576546 | Rare:56 | ||||
chr11:615948-616108 | Common:1; Rare:50 | ||||
chr11:695535-695817 | Common:1; Rare:74 | ||||
chr11:747289-747514 | Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777455-777593 | Common:1; Rare:59 | ||||
chr11:805189-805412 | Common:5; Rare:94 | ||||
chr11:809503-809647 | Common:2; Rare:38 |