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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
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      <PRIMARY_ID>SRX18377977</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756060_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756060: OMM2.3_IgG_CST; Homo sapiens; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409779</PRIMARY_ID>
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        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were fixed with 1% formaldehyde for 10 minutes. After quenching and cell lysis, chromatin was sonicated using an ultrasonicator (Thermo Fisher). ChIP-seq libraries were constructed by Novogene Corporation (Beijing, China). DNA purity was checked using the NanoPhotometer® spectrophotometer (IMPLEN, CA, USA). DNA concentration was measured using Qubit® DNA Assay Kit in Qubit® 3.0Flurometer(LifeTechnologies,CA,USA). Pair-end sequencing of sample was performed on Illumina platform (Illumina, CA, USA). Library quality was assessed on the Agilent Bioanalyzer 2100 system.</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX18377978</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756061_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756061: OMM2.3_A3B_ABCAM; Homo sapiens; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409779</PRIMARY_ID>
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        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were fixed with 1% formaldehyde for 10 minutes. After quenching and cell lysis, chromatin was sonicated using an ultrasonicator (Thermo Fisher). ChIP-seq libraries were constructed by Novogene Corporation (Beijing, China). DNA purity was checked using the NanoPhotometer® spectrophotometer (IMPLEN, CA, USA). DNA concentration was measured using Qubit® DNA Assay Kit in Qubit® 3.0Flurometer(LifeTechnologies,CA,USA). Pair-end sequencing of sample was performed on Illumina platform (Illumina, CA, USA). Library quality was assessed on the Agilent Bioanalyzer 2100 system.</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX18377979</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756062_r1</EXTERNAL_ID>
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    <TITLE>GSM6756062: 92.1_IgG_CST; Homo sapiens; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409779</PRIMARY_ID>
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        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were fixed with 1% formaldehyde for 10 minutes. After quenching and cell lysis, chromatin was sonicated using an ultrasonicator (Thermo Fisher). ChIP-seq libraries were constructed by Novogene Corporation (Beijing, China). DNA purity was checked using the NanoPhotometer® spectrophotometer (IMPLEN, CA, USA). DNA concentration was measured using Qubit® DNA Assay Kit in Qubit® 3.0Flurometer(LifeTechnologies,CA,USA). Pair-end sequencing of sample was performed on Illumina platform (Illumina, CA, USA). Library quality was assessed on the Agilent Bioanalyzer 2100 system.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX18377980</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756063_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756063: 92.1_A3B_ABCAM; Homo sapiens; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409779</PRIMARY_ID>
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        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were fixed with 1% formaldehyde for 10 minutes. After quenching and cell lysis, chromatin was sonicated using an ultrasonicator (Thermo Fisher). ChIP-seq libraries were constructed by Novogene Corporation (Beijing, China). DNA purity was checked using the NanoPhotometer® spectrophotometer (IMPLEN, CA, USA). DNA concentration was measured using Qubit® DNA Assay Kit in Qubit® 3.0Flurometer(LifeTechnologies,CA,USA). Pair-end sequencing of sample was performed on Illumina platform (Illumina, CA, USA). Library quality was assessed on the Agilent Bioanalyzer 2100 system.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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