Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:207381-207598 | Common:5; Rare:79 | ||||
chr11:208756-208821 | Rare:19 | ||||
chr11:236891-237055 | Common:1; Rare:62 | ||||
chr11:777467-777593 | Rare:53 | ||||
chr11:842478-842832 | Common:7; Rare:157 | ||||
chr11:843939-844153 | Common:1; Rare:55 | ||||
chr11:3797521-3797742 | Rare:79 | ||||
chr11:5624903-5625023 | Rare:15 | ||||
chr11:6481302-6481524 | Common:4; Rare:88 | ||||
chr11:6603586-6603820 | Common:2; Rare:72; Clinvar (benign):3 | ||||
chr11:6683261-6683611 | Common:6; Rare:141 | ||||
chr11:8682638-8682816 | Common:2; Rare:79 | ||||
chr11:8964401-8964518 | Common:3; Rare:34 | ||||
chr11:9460778-9461030 | Common:2; Rare:76 | ||||
chr11:10304872-10305083 | Common:1; Rare:48 |