Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:307579-307790 | Common:6; Rare:61 | ||||
chr11:320566-320924 | Common:5; Rare:139; Clinvar:1 | ||||
chr11:417330-417480 | Rare:38 | ||||
chr11:506732-507001 | Common:3; Rare:92 | ||||
chr11:507135-507268 | Rare:47 | ||||
chr11:535429-535743 | Common:5; Rare:130; Clinvar (benign):1 | ||||
chr11:537322-537533 | Common:5; Rare:65 | ||||
chr11:560710-561021 | Common:5; Rare:143 | ||||
chr11:576431-576531 | Rare:40 | ||||
chr11:695731-695821 | Rare:30 | ||||
chr11:747251-747514 | Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777465-777598 | Common:1; Rare:58 | ||||
chr11:809502-809655 | Common:2; Rare:41 | ||||
chr11:809796-810038 | Common:2; Rare:111 | ||||
chr11:825930-826253 | Rare:78 |