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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="ERX4439541" alias="SC_EXP_30560_1#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439541</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:A4, constructed from sample accession ERS3559079 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence AATCGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559079">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559079</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755624</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="152" NOMINAL_SDEV="54"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439542" alias="SC_EXP_30560_1#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439542</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:B4, constructed from sample accession ERS3559080 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GTCTACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559080">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559080</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755625</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="147" NOMINAL_SDEV="49"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439543" alias="SC_EXP_30560_1#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439543</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:C4, constructed from sample accession ERS3559081 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CGCTGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559081">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559081</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755626</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="147" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439544" alias="SC_EXP_30560_1#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439544</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:D4, constructed from sample accession ERS3559082 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GATCAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559082">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559082</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="146" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439545" alias="SC_EXP_30560_1#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439545</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E4, constructed from sample accession ERS3559083 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CGAAGGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559083">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559083</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755628</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="157" NOMINAL_SDEV="59"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439546" alias="SC_EXP_30560_1#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439546</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F4, constructed from sample accession ERS3559084 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GATGCCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559084">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559084</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755629</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="151" NOMINAL_SDEV="54"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439547" alias="SC_EXP_30560_1#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439547</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G4, constructed from sample accession ERS3559085 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CTACGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559085">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559085</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755630</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="147" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439548" alias="SC_EXP_30560_1#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439548</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H4, constructed from sample accession ERS3559086 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GATGCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559086">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559086</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755631</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="141" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439549" alias="SC_EXP_30560_1#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439549</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:A5, constructed from sample accession ERS3559087 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CTACGGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559087">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559087</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="146" NOMINAL_SDEV="49"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439550" alias="SC_EXP_30560_1#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439550</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:B5, constructed from sample accession ERS3559088 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GATTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559088">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559088</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755633</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="142" NOMINAL_SDEV="46"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439551" alias="SC_EXP_30560_1#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439551</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:C5, constructed from sample accession ERS3559089 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CTACTCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559089">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559089</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755634</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="142" NOMINAL_SDEV="46"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439552" alias="SC_EXP_30560_1#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439552</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:D5, constructed from sample accession ERS3559090 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GATTCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559090">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559090</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="142" NOMINAL_SDEV="46"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439553" alias="SC_EXP_30560_1#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439553</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E5, constructed from sample accession ERS3559091 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence AATCGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559091">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559091</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755636</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="158" NOMINAL_SDEV="59"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439554" alias="SC_EXP_30560_1#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439554</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F5, constructed from sample accession ERS3559092 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence TTCGCCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559092">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559092</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="148" NOMINAL_SDEV="48"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439555" alias="SC_EXP_30560_1#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439555</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G5, constructed from sample accession ERS3559093 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CTGGCCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559093">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559093</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="146" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439556" alias="SC_EXP_30560_1#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439556</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H5, constructed from sample accession ERS3559094 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GAACTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559094">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559094</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755639</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="150" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439557" alias="SC_EXP_30560_1#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439557</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:A6, constructed from sample accession ERS3559095 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CGTATTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559095">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559095</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755640</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="150" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439558" alias="SC_EXP_30560_1#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439558</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:B6, constructed from sample accession ERS3559096 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GAAGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559096">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559096</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="153" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439559" alias="SC_EXP_30560_1#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439559</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:C6, constructed from sample accession ERS3559097 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CTTAATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559097">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559097</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755642</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="159" NOMINAL_SDEV="56"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439560" alias="SC_EXP_30560_1#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439560</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:D6, constructed from sample accession ERS3559098 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GAAGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559098">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559098</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755643</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="154" NOMINAL_SDEV="56"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439561" alias="SC_EXP_30560_1#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439561</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E6, constructed from sample accession ERS3559099 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GAAGAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559099">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559099</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="153" NOMINAL_SDEV="57"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439562" alias="SC_EXP_30560_1#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439562</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F6, constructed from sample accession ERS3559100 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CGGATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559100">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559100</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755645</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="144" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439563" alias="SC_EXP_30560_1#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439563</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G6, constructed from sample accession ERS3559101 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GAATCTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559101">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559101</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="150" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439564" alias="SC_EXP_30560_1#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439564</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H6, constructed from sample accession ERS3559102 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CTGATTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559102">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559102</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755647</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="149" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439565" alias="SC_EXP_30560_1#25">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439565</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:A7, constructed from sample accession ERS3559103 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence AATCCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559103">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559103</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755648</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="159" NOMINAL_SDEV="61"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439566" alias="SC_EXP_30560_1#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439566</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:B7, constructed from sample accession ERS3559104 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence TGCGTACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559104">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559104</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755649</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="149" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439567" alias="SC_EXP_30560_1#27">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439567</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:C7, constructed from sample accession ERS3559105 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GAATCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559105">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559105</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755650</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="144" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439568" alias="SC_EXP_30560_1#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439568</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:D7, constructed from sample accession ERS3559106 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence TGAGTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559106">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559106</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755651</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="147" NOMINAL_SDEV="49"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439569" alias="SC_EXP_30560_1#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439569</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E7, constructed from sample accession ERS3559107 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GAATGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559107">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559107</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" NOMINAL_SDEV="59"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439570" alias="SC_EXP_30560_1#30">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439570</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F7, constructed from sample accession ERS3559108 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GAATATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559108">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755653</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="151" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439571" alias="SC_EXP_30560_1#31">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439571</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G7, constructed from sample accession ERS3559109 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CTTATGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559109">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755654</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="141" NOMINAL_SDEV="42"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439572" alias="SC_EXP_30560_1#32">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439572</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H7, constructed from sample accession ERS3559110 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence TCGGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559110">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559110</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755655</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="144" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439573" alias="SC_EXP_30560_1#33">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439573</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:A8, constructed from sample accession ERS3559111 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence AAGAAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559111">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559111</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755656</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="161" NOMINAL_SDEV="62"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439574" alias="SC_EXP_30560_1#34">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439574</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:B8, constructed from sample accession ERS3559112 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CTCACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559112">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559112</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755657</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="145" NOMINAL_SDEV="48"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439575" alias="SC_EXP_30560_1#35">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439575</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:C8, constructed from sample accession ERS3559113 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence TCGGTCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559113">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559113</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755658</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="149" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439576" alias="SC_EXP_30560_1#36">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439576</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:D8, constructed from sample accession ERS3559114 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence TCGGTAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559114">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559114</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755659</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="147" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439577" alias="SC_EXP_30560_1#37">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439577</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E8, constructed from sample accession ERS3559115 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence AAGATACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559115">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559115</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755660</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="160" NOMINAL_SDEV="59"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439578" alias="SC_EXP_30560_1#38">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439578</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F8, constructed from sample accession ERS3559116 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence GTCGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559116">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559116</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755661</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" NOMINAL_SDEV="56"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439579" alias="SC_EXP_30560_1#39">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439579</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G8, constructed from sample accession ERS3559117 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence TCGGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559117">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559117</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755662</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" NOMINAL_SDEV="57"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439580" alias="SC_EXP_30560_1#40">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439580</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H8, constructed from sample accession ERS3559118 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CGAGCCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559118">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559118</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755663</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="156" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439581" alias="SC_EXP_30560_1#41">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439581</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:A9, constructed from sample accession ERS3559119 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CGATTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559119">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755664</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="151" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439582" alias="SC_EXP_30560_1#42">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439582</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:B9, constructed from sample accession ERS3559120 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence TCGAAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559120">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755665</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="134" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439583" alias="SC_EXP_30560_1#43">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439583</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:C9, constructed from sample accession ERS3559121 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CTATCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559121">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755666</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="131" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439584" alias="SC_EXP_30560_1#44">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439584</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:D9, constructed from sample accession ERS3559122 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CGCGCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559122">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559122</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755667</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="133" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439585" alias="SC_EXP_30560_1#45">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439585</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E9, constructed from sample accession ERS3559123 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CGAACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559123">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559123</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755668</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" NOMINAL_SDEV="57"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439586" alias="SC_EXP_30560_1#46">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439586</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F9, constructed from sample accession ERS3559124 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CTACTGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559124">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559124</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755669</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="149" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439587" alias="SC_EXP_30560_1#47">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439587</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G9, constructed from sample accession ERS3559125 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence TCTTAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559125">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559125</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755670</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="154" NOMINAL_SDEV="55"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439588" alias="SC_EXP_30560_1#48">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439588</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H9, constructed from sample accession ERS3559126 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence TTAGAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559126">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559126</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755671</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="153" NOMINAL_SDEV="56"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439589" alias="SC_EXP_30560_1#49">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439589</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E10, constructed from sample accession ERS3559127 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559127">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559127</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755672</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="157" NOMINAL_SDEV="42"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439590" alias="SC_EXP_30560_1#50">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439590</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F10, constructed from sample accession ERS3559128 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence TCACCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559128">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559128</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755673</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="150" NOMINAL_SDEV="42"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439591" alias="SC_EXP_30560_1#51">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439591</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G10, constructed from sample accession ERS3559129 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CTGGAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559129">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559129</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755674</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" NOMINAL_SDEV="36"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439592" alias="SC_EXP_30560_1#52">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439592</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_1#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_1#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H10, constructed from sample accession ERS3559130 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_1).  This submission includes reads tagged with the sequence CGTAAGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559130">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559130</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755675</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="152" NOMINAL_SDEV="42"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439593" alias="SC_EXP_30560_2#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439593</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:A4, constructed from sample accession ERS3559079 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence AATCGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559079">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559079</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755624</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="150" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439594" alias="SC_EXP_30560_2#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439594</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:B4, constructed from sample accession ERS3559080 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GTCTACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559080">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559080</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755625</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="147" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439595" alias="SC_EXP_30560_2#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439595</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:C4, constructed from sample accession ERS3559081 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CGCTGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559081">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559081</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755626</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="148" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439596" alias="SC_EXP_30560_2#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439596</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:D4, constructed from sample accession ERS3559082 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GATCAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559082">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559082</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="146" NOMINAL_SDEV="49"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439597" alias="SC_EXP_30560_2#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439597</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E4, constructed from sample accession ERS3559083 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CGAAGGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559083">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559083</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755628</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="156" NOMINAL_SDEV="57"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439598" alias="SC_EXP_30560_2#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439598</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F4, constructed from sample accession ERS3559084 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GATGCCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559084">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559084</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755629</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="152" NOMINAL_SDEV="55"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439599" alias="SC_EXP_30560_2#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439599</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G4, constructed from sample accession ERS3559085 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CTACGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559085">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559085</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755630</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="147" NOMINAL_SDEV="49"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439600" alias="SC_EXP_30560_2#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439600</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H4, constructed from sample accession ERS3559086 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GATGCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559086">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559086</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755631</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="143" NOMINAL_SDEV="46"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439601" alias="SC_EXP_30560_2#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439601</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:A5, constructed from sample accession ERS3559087 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CTACGGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559087">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559087</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="148" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439602" alias="SC_EXP_30560_2#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439602</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:B5, constructed from sample accession ERS3559088 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GATTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559088">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559088</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755633</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="141" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439603" alias="SC_EXP_30560_2#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439603</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:C5, constructed from sample accession ERS3559089 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CTACTCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559089">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559089</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755634</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="144" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439604" alias="SC_EXP_30560_2#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439604</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:D5, constructed from sample accession ERS3559090 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GATTCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559090">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559090</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="143" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439605" alias="SC_EXP_30560_2#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439605</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E5, constructed from sample accession ERS3559091 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence AATCGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559091">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559091</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755636</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="159" NOMINAL_SDEV="60"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439606" alias="SC_EXP_30560_2#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439606</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F5, constructed from sample accession ERS3559092 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence TTCGCCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559092">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559092</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="148" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439607" alias="SC_EXP_30560_2#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439607</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G5, constructed from sample accession ERS3559093 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CTGGCCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559093">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559093</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="146" NOMINAL_SDEV="48"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439608" alias="SC_EXP_30560_2#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439608</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H5, constructed from sample accession ERS3559094 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GAACTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559094">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559094</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755639</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="152" NOMINAL_SDEV="54"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439609" alias="SC_EXP_30560_2#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439609</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:A6, constructed from sample accession ERS3559095 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CGTATTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559095">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559095</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755640</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="152" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439610" alias="SC_EXP_30560_2#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439610</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:B6, constructed from sample accession ERS3559096 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GAAGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559096">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559096</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="154" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439611" alias="SC_EXP_30560_2#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439611</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:C6, constructed from sample accession ERS3559097 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CTTAATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559097">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559097</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755642</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="158" NOMINAL_SDEV="59"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439612" alias="SC_EXP_30560_2#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439612</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:D6, constructed from sample accession ERS3559098 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GAAGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559098">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559098</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755643</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="154" NOMINAL_SDEV="57"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439613" alias="SC_EXP_30560_2#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439613</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E6, constructed from sample accession ERS3559099 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GAAGAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559099">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559099</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="154" NOMINAL_SDEV="56"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439614" alias="SC_EXP_30560_2#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439614</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F6, constructed from sample accession ERS3559100 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CGGATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559100">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559100</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755645</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="144" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439615" alias="SC_EXP_30560_2#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439615</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G6, constructed from sample accession ERS3559101 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GAATCTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559101">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559101</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="148" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439616" alias="SC_EXP_30560_2#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439616</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H6, constructed from sample accession ERS3559102 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CTGATTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559102">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559102</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755647</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="149" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439617" alias="SC_EXP_30560_2#25">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439617</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:A7, constructed from sample accession ERS3559103 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence AATCCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559103">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559103</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755648</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="156" NOMINAL_SDEV="59"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439618" alias="SC_EXP_30560_2#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439618</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:B7, constructed from sample accession ERS3559104 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence TGCGTACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559104">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559104</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755649</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="150" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439619" alias="SC_EXP_30560_2#27">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439619</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:C7, constructed from sample accession ERS3559105 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GAATCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559105">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559105</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755650</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="145" NOMINAL_SDEV="46"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439620" alias="SC_EXP_30560_2#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439620</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:D7, constructed from sample accession ERS3559106 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence TGAGTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559106">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559106</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755651</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="147" NOMINAL_SDEV="49"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439621" alias="SC_EXP_30560_2#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439621</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E7, constructed from sample accession ERS3559107 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GAATGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559107">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559107</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" NOMINAL_SDEV="59"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439622" alias="SC_EXP_30560_2#30">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439622</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F7, constructed from sample accession ERS3559108 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GAATATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559108">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755653</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="152" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439623" alias="SC_EXP_30560_2#31">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439623</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G7, constructed from sample accession ERS3559109 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CTTATGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559109">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755654</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="141" NOMINAL_SDEV="42"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439624" alias="SC_EXP_30560_2#32">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439624</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H7, constructed from sample accession ERS3559110 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence TCGGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559110">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559110</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755655</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="143" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439625" alias="SC_EXP_30560_2#33">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439625</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:A8, constructed from sample accession ERS3559111 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence AAGAAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559111">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559111</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755656</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="161" NOMINAL_SDEV="62"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439626" alias="SC_EXP_30560_2#34">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439626</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:B8, constructed from sample accession ERS3559112 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CTCACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559112">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559112</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755657</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="147" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439627" alias="SC_EXP_30560_2#35">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439627</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:C8, constructed from sample accession ERS3559113 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence TCGGTCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559113">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559113</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755658</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="151" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439628" alias="SC_EXP_30560_2#36">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439628</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:D8, constructed from sample accession ERS3559114 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence TCGGTAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559114">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559114</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755659</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="148" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439629" alias="SC_EXP_30560_2#37">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439629</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E8, constructed from sample accession ERS3559115 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence AAGATACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559115">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559115</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755660</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="161" NOMINAL_SDEV="61"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439630" alias="SC_EXP_30560_2#38">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439630</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F8, constructed from sample accession ERS3559116 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence GTCGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559116">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559116</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755661</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" NOMINAL_SDEV="55"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439631" alias="SC_EXP_30560_2#39">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439631</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G8, constructed from sample accession ERS3559117 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence TCGGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559117">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559117</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755662</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="157" NOMINAL_SDEV="56"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439632" alias="SC_EXP_30560_2#40">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439632</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H8, constructed from sample accession ERS3559118 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CGAGCCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559118">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559118</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755663</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" NOMINAL_SDEV="55"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439633" alias="SC_EXP_30560_2#41">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439633</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:A9, constructed from sample accession ERS3559119 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CGATTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559119">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755664</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="151" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439634" alias="SC_EXP_30560_2#42">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439634</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:B9, constructed from sample accession ERS3559120 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence TCGAAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559120">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755665</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="134" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439635" alias="SC_EXP_30560_2#43">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439635</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:C9, constructed from sample accession ERS3559121 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CTATCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559121">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755666</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="131" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439636" alias="SC_EXP_30560_2#44">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439636</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:D9, constructed from sample accession ERS3559122 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CGCGCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559122">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559122</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755667</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="133" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439637" alias="SC_EXP_30560_2#45">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439637</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E9, constructed from sample accession ERS3559123 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CGAACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559123">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559123</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755668</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="153" NOMINAL_SDEV="56"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439638" alias="SC_EXP_30560_2#46">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439638</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F9, constructed from sample accession ERS3559124 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CTACTGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559124">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559124</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755669</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="150" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439639" alias="SC_EXP_30560_2#47">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439639</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G9, constructed from sample accession ERS3559125 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence TCTTAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559125">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559125</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755670</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" NOMINAL_SDEV="54"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439640" alias="SC_EXP_30560_2#48">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439640</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H9, constructed from sample accession ERS3559126 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence TTAGAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559126">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559126</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755671</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="152" NOMINAL_SDEV="57"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439641" alias="SC_EXP_30560_2#49">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439641</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:E10, constructed from sample accession ERS3559127 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559127">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559127</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755672</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="157" NOMINAL_SDEV="40"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439642" alias="SC_EXP_30560_2#50">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439642</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:F10, constructed from sample accession ERS3559128 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence TCACCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559128">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559128</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755673</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="151" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439643" alias="SC_EXP_30560_2#51">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439643</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:G10, constructed from sample accession ERS3559129 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CTGGAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559129">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559129</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755674</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" NOMINAL_SDEV="42"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4439644" alias="SC_EXP_30560_2#52">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4439644</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30560_2#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30560_2#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004361">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004361</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB5007</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN584484I:H10, constructed from sample accession ERS3559130 for study accession ERP004361.  This is part of an Illumina multiplexed sequencing run (30560_2).  This submission includes reads tagged with the sequence CGTAAGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3559130">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3559130</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5755675</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN584484I:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="152" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
