Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:560710-561008 | Common:5; Rare:140 | ||||
chr11:576431-576531 | Rare:40 | ||||
chr11:615946-616006 | Rare:14 | ||||
chr11:695756-695818 | Rare:24 | ||||
chr11:777465-777616 | Common:1; Rare:67 | ||||
chr11:826043-826169 | Rare:31 | ||||
chr11:832826-833022 | Common:7; Rare:65 | ||||
chr11:842471-842899 | Common:7; Rare:177 | ||||
chr11:843965-844165 | Common:1; Rare:48 | ||||
chr11:1486758-1487027 | Common:1; Rare:45 | ||||
chr11:1838697-1839032 | Common:2; Rare:89; Clinvar:1 | ||||
chr11:1876348-1876502 | Rare:32 | ||||
chr11:1919444-1919756 | Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
chr11:1921291-1921441 | Common:2; Rare:26 | ||||
chr11:1922612-1922877 | Common:1; Rare:74 |