Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:61362276-61362415 | Common:1; Rare:40; Clinvar:6 | ||||
chr11:61392527-61392652 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
chr11:61429929-61430152 | Common:1; Rare:99; Clinvar:1; Clinvar (benign):3 | ||||
chr11:61792564-61792955 | Common:5; Rare:108 | ||||
chr11:61816765-61816971 | Rare:62 | ||||
chr11:61967615-61967759 | Common:1; Rare:55; Clinvar:3 | ||||
chr11:62665109-62665317 | Common:4; Rare:94 | ||||
chr11:62671821-62671902 | Rare:30 | ||||
chr11:62679026-62679196 | Rare:55 | ||||
chr11:62706228-62706405 | Common:3; Rare:74; Clinvar (benign):5 | ||||
chr11:62707304-62707694 | Common:4; Rare:82 | ||||
chr11:62761337-62761619 | Common:1; Rare:75 | ||||
chr11:62832042-62832244 | Rare:70 | ||||
chr11:62841807-62842079 | Common:6; Rare:116 | ||||
chr11:62855878-62856169 | Rare:108 |