Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:327278-327304 | Rare:6 | ||||
chr11:407107-407408 | Common:8; Rare:91 | ||||
chr11:414939-415191 | Common:1; Rare:56 | ||||
chr11:506737-506994 | Common:3; Rare:87 | ||||
chr11:537339-537552 | Common:4; Rare:71 | ||||
chr11:560704-561003 | Common:6; Rare:139 | ||||
chr11:576431-576542 | Rare:47 | ||||
chr11:615622-615785 | Rare:60 | ||||
chr11:695752-695821 | Rare:26 | ||||
chr11:747315-747493 | Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777460-777614 | Common:1; Rare:68 | ||||
chr11:797952-798086 | Common:1; Rare:42 | ||||
chr11:809795-810356 | Common:3; Rare:237 | ||||
chr11:812531-812734 | Common:1; Rare:77 | ||||
chr11:832891-833014 | Common:6; Rare:46 |