file: liu2026Multiomics-supplentary-tables.xlsx
format: excel
meta:
  description: '| column_name      | column_description                                            |

    | ---------------- | -------------------------------------------------------------
    |

    | `meta_ID`        | CAUSALdb unique ID for trait                                  |

    | `MeSH_ID`        | Medical Subject Headings ID for trait                         |

    | `trait_name`     | Name of trait                                                 |

    | `fetal_celltype` | Fetal cell type enriched with variants from indicated trait   |

    | `z`              | Z score of gchromVAR enrichment                               |

    | `p`              | p value of gchromVAR enrichment                               |

    | `FDR`            | False discovery rate (Benjamini-Hochberg adjusted p value)    |

    | `organ`          | Organ the fetal cell type is found in                         |'
  summary: g-chromVAR results, related to Fig. 6
  labels:
    assay: SHARE-seq
    vendor: unknown
    sequencing_platform: Illumina
    dataset: liu2026Multiomics
    reference_genome: reference/Human/genome/ucsc-hg38
    species: human
parameters:
  sheet_name: S9
type: data_frame