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VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases.

, , , , , , , , , and . Nucleic Acids Res., 50 (D1): 1408-1416 (2022)

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VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases., , , , , , , , , and . Nucleic Acids Res., 50 (D1): 1408-1416 (2022)Inferring CTCF-binding patterns and anchored loops across human tissues and cell types., , , , , , , , , and 11 other author(s). Patterns, 4 (8): 100798 (August 2023)GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits., , , , , , , , and . Nucleic Acids Res., 46 (Webserver-Issue): W114-W120 (2018)QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes., , , , , , , , , and 5 other author(s). Nucleic Acids Res., 48 (Database-Issue): D983-D991 (2020)QTLbase2: an enhanced catalog of human quantitative trait loci on extensive molecular phenotypes., , , , , , , , , and 2 other author(s). Nucleic Acids Res., 51 (D1): 1122-1128 (January 2023)CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies., , , , , , , , , and 8 other author(s). Nucleic Acids Res., 48 (Database-Issue): D807-D816 (2020)