Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:34916287-34916650 | Common:9; Rare:148; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
chr11:46846248-46846394 | Rare:39 | ||||
chr11:47270015-47270177 | Common:1; Rare:58 | ||||
chr11:47565478-47565635 | Common:3; Rare:30 | ||||
chr11:47578968-47579085 | Rare:60; Clinvar:2 | ||||
chr11:57567612-57567732 | Rare:41 | ||||
chr11:59142689-59142859 | Rare:24 | ||||
chr11:60952336-60952512 | Rare:40 | ||||
chr11:61333053-61333207 | Rare:51 | ||||
chr11:61362278-61362397 | Common:1; Rare:34; Clinvar:5 | ||||
chr11:61429957-61430144 | Common:1; Rare:79; Clinvar (benign):2 | ||||
chr11:61792573-61792951 | Common:5; Rare:101 | ||||
chr11:62665165-62665317 | Common:4; Rare:64 | ||||
chr11:62679018-62679197 | Rare:61 | ||||
chr11:62761366-62761608 | Common:1; Rare:64 |