Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:47269566-47269685 | Common:1; Rare:40 | ||||
chr11:47269981-47270166 | Common:1; Rare:61 | ||||
chr11:47565499-47565620 | Common:3; Rare:23 | ||||
chr11:47578968-47579085 | Rare:60; Clinvar:2 | ||||
chr11:57712184-57712643 | Common:9; Rare:154 | ||||
chr11:59142762-59142864 | Rare:17 | ||||
chr11:60841864-60842135 | Common:2; Rare:92 | ||||
chr11:61333028-61333240 | Rare:70 | ||||
chr11:61361874-61362039 | Common:1; Rare:38 | ||||
chr11:61362246-61362400 | Common:2; Rare:45; Clinvar:7; Clinvar (benign):1 | ||||
chr11:61392527-61392649 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
chr11:61429921-61430141 | Common:1; Rare:98; Clinvar (benign):2 | ||||
chr11:61792567-61792955 | Common:5; Rare:105 | ||||
chr11:61967311-61967806 | Common:3; Rare:185; Clinvar:4 | ||||
chr11:62545620-62545975 | Common:1; Rare:78 |