<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM5342115" accession="SRX11001632">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11001632</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5342115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5342115: ChIPseq_Raw264.7_DexLPS_GR; Mus musculus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP321494" refname="GSE175582">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP321494</PRIMARY_ID>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS9075962</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5342115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>20 million cells were then harvested for each ChIP assay. The experimental procedure for ChIP was as previously described (Barish et al., 2010). Briefly, after fixation, nuclei from were isolated, lysed, and sheared with a Covaris Ultrasonicator ME220 to yield DNA fragment sizes of 200–1,000 bp followed by immunoprecipitation. libraries were prepared for sequencing using standard Illumina protocols.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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          <DB>gds</DB>
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          <LABEL>GSM5342115</LABEL>
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    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5342115</VALUE>
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    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5342116" accession="SRX11001633">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11001633</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5342116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5342116: ChIPseq_Raw264.7_DexLPS_dBRD9_GR; Mus musculus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP321494" refname="GSE175582">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP321494</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS9075963">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9075963</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5342116</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>20 million cells were then harvested for each ChIP assay. The experimental procedure for ChIP was as previously described (Barish et al., 2010). Briefly, after fixation, nuclei from were isolated, lysed, and sheared with a Covaris Ultrasonicator ME220 to yield DNA fragment sizes of 200–1,000 bp followed by immunoprecipitation. libraries were prepared for sequencing using standard Illumina protocols.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305342116</ID>
          <LABEL>GSM5342116</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5342116</VALUE>
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    </EXPERIMENT_ATTRIBUTES>
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</EXPERIMENT_SET>
