Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:58578119-58578211 | Rare:24 | ||||
chr11:59142756-59142879 | Rare:20 | ||||
chr11:59212889-59213143 | Common:1; Rare:70 | ||||
chr11:59810666-59810900 | Common:3; Rare:80 | ||||
chr11:60378389-60378540 | Rare:19 | ||||
chr11:60455526-60455945 | Common:3; Rare:78 | ||||
chr11:60906414-60906600 | Rare:49 | ||||
chr11:60914149-60914229 | Rare:22 | ||||
chr11:60952130-60952294 | Common:1; Rare:35 | ||||
chr11:61333045-61333266 | Rare:77 | ||||
chr11:61361851-61362023 | Common:1; Rare:39 | ||||
chr11:61362200-61362404 | Common:2; Rare:61; Clinvar:8; Clinvar (benign):1 | ||||
chr11:61392527-61392649 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
chr11:61429920-61430159 | Common:1; Rare:109; Clinvar:2; Clinvar (benign):4 | ||||
chr11:61792568-61792955 | Common:5; Rare:105 |