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        <identifier>oai:researchdata.se:doi-10-17044-scilifelab-24260710/0</identifier>
        <datestamp>2023-11-24</datestamp>
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          <dc:identifier>https://doi.org/10.17044/SCILIFELAB.24260710</dc:identifier>
          <dc:title xml:lang="en">Activating mutations remodeled the chromatin accessibility landscape to drive distinct regulatory networks in KMT2A-rearranged acute leukemia associated with immune evasion</dc:title>
          <dc:creator>Qirui Zhang</dc:creator>
          <dc:creator>https://orcid.org/0000-0002-5341-4472</dc:creator>
          <dc:creator>https://orcid.org/0000-0002-9235-1953</dc:creator>
          <dc:creator>Helena Sturesson</dc:creator>
          <dc:creator>Anders Castor</dc:creator>
          <dc:creator>Hanne V. Marquart</dc:creator>
          <dc:creator>Birgitte Lausen</dc:creator>
          <dc:creator>Axel Hyrenius Wittsten</dc:creator>
          <dc:creator>Anna Hagström Andersson</dc:creator>
          <dc:subject xml:lang="en">Medical and Health Sciences</dc:subject>
          <dc:subject xml:lang="sv">Medicin och hälsovetenskap</dc:subject>
          <dc:subject xml:lang="en">Biological Sciences</dc:subject>
          <dc:subject xml:lang="sv">Biologi</dc:subject>
          <dc:description xml:lang="en">This dataset includes ATAC-seq (Assay for Transposase-Accessible Chromatin using sequencing) of five infants with acute lymphoblastic leukemia. All patients had an underlying rearrangement of the KMT2A genes, either KMT2A::MLLT1 (n=1), KMT2A::AFF1 (n=3), or KMT2A::MLLT10 (n=1). Three patients also had activating mutations of NRAS G13D and/or KRAS G12D. The median age of the cohort was 2 months 7 days. Diagnostic sample from bone marrow underwent the ATAC-seq library preparation and sequenced on the NextSeq 500 platform (Illumina, San Diego, CA, USA).</dc:description>
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          <dc:publisher xml:lang="en">Lund University</dc:publisher>
          <dc:publisher xml:lang="sv">Lunds universitet</dc:publisher>
          <dc:date>2023-11-24T00:00:00Z</dc:date>
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