Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:46237215-46237389 | Rare:26 | ||||
chr11:46428999-46429053 | Rare:11 | ||||
chr11:47186977-47187115 | Rare:28 | ||||
chr11:48065911-48066041 | Common:1; Rare:24 | ||||
chr11:57332416-57332689 | Rare:61 | ||||
chr11:57638235-57638380 | Rare:32 | ||||
chr11:57738374-57738695 | Rare:84 | ||||
chr11:57778585-57778834 | Rare:43 | ||||
chr11:59545383-59545626 | Rare:57 | ||||
chr11:59549302-59549327 | Rare:6 | ||||
chr11:59550693-59550837 | Common:3; Rare:64 | ||||
chr11:60900590-60900880 | Common:1; Rare:64 | ||||
chr11:62140754-62140975 | Common:1; Rare:72 | ||||
chr11:62544689-62544818 | Rare:30 | ||||
chr11:64223149-64223534 | Common:1; Rare:131; Clinvar:3; Clinvar (benign):2 |