<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX23780460" alias="GSM8117802_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23780460</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8117802_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8117802: sgNT_5hmC_input; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP492323">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP492323</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1081832</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20604533">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20604533</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8117802</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8117802</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA were extracted and sheared into fragments with an average size of 200 bp. 60 μg sonicated genomic DNA used in glucose transfer reaction and then proceeded biotinylation reaction. DNA were captured by Dynabeads Myone Streptavidin C1 (Invitrogen™ 65001) and libraries were prepared. Libraries were prepared by using NEBNext1100 ® Ultra™ II DNA Library Prep kit (NEB, E7103) Illuminal NextSeq 2000 P2 100cycles</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23780461" alias="GSM8117803_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23780461</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8117803_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8117803: sgNT_5hmC_ChIPed_1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP492323">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP492323</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1081832</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20605280">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20605280</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8117803</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8117803</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA were extracted and sheared into fragments with an average size of 200 bp. 60 μg sonicated genomic DNA used in glucose transfer reaction and then proceeded biotinylation reaction. DNA were captured by Dynabeads Myone Streptavidin C1 (Invitrogen™ 65001) and libraries were prepared. Libraries were prepared by using NEBNext1100 ® Ultra™ II DNA Library Prep kit (NEB, E7103) Illuminal NextSeq 2000 P2 100cycles</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23780462" alias="GSM8117804_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23780462</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8117804_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8117804: sgNT_5hmC_ChIPed_2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP492323">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP492323</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1081832</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20604534">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20604534</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8117804</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8117804</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA were extracted and sheared into fragments with an average size of 200 bp. 60 μg sonicated genomic DNA used in glucose transfer reaction and then proceeded biotinylation reaction. DNA were captured by Dynabeads Myone Streptavidin C1 (Invitrogen™ 65001) and libraries were prepared. Libraries were prepared by using NEBNext1100 ® Ultra™ II DNA Library Prep kit (NEB, E7103) Illuminal NextSeq 2000 P2 100cycles</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23780463" alias="GSM8117805_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23780463</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8117805_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8117805: sgZNF397_5hmC_input; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP492323">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP492323</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1081832</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20604535">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20604535</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8117805</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8117805</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA were extracted and sheared into fragments with an average size of 200 bp. 60 μg sonicated genomic DNA used in glucose transfer reaction and then proceeded biotinylation reaction. DNA were captured by Dynabeads Myone Streptavidin C1 (Invitrogen™ 65001) and libraries were prepared. Libraries were prepared by using NEBNext1100 ® Ultra™ II DNA Library Prep kit (NEB, E7103) Illuminal NextSeq 2000 P2 100cycles</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23780464" alias="GSM8117806_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23780464</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8117806_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8117806: sgZNF397_5hmC_ChIPed_1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP492323">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP492323</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1081832</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20605963">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20605963</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8117806</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8117806</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA were extracted and sheared into fragments with an average size of 200 bp. 60 μg sonicated genomic DNA used in glucose transfer reaction and then proceeded biotinylation reaction. DNA were captured by Dynabeads Myone Streptavidin C1 (Invitrogen™ 65001) and libraries were prepared. Libraries were prepared by using NEBNext1100 ® Ultra™ II DNA Library Prep kit (NEB, E7103) Illuminal NextSeq 2000 P2 100cycles</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23780465" alias="GSM8117807_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23780465</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8117807_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8117807: sgZNF397_5hmC_ChIPed_2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP492323">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP492323</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1081832</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20604536">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20604536</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8117807</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8117807</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA were extracted and sheared into fragments with an average size of 200 bp. 60 μg sonicated genomic DNA used in glucose transfer reaction and then proceeded biotinylation reaction. DNA were captured by Dynabeads Myone Streptavidin C1 (Invitrogen™ 65001) and libraries were prepared. Libraries were prepared by using NEBNext1100 ® Ultra™ II DNA Library Prep kit (NEB, E7103) Illuminal NextSeq 2000 P2 100cycles</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23780466" alias="GSM8117808_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23780466</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8117808_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8117808: sgZNF397_sgTET2_5hmC_input; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP492323">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP492323</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1081832</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20604537">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20604537</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8117808</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8117808</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA were extracted and sheared into fragments with an average size of 200 bp. 60 μg sonicated genomic DNA used in glucose transfer reaction and then proceeded biotinylation reaction. DNA were captured by Dynabeads Myone Streptavidin C1 (Invitrogen™ 65001) and libraries were prepared. Libraries were prepared by using NEBNext1100 ® Ultra™ II DNA Library Prep kit (NEB, E7103) Illuminal NextSeq 2000 P2 100cycles</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23780467" alias="GSM8117809_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23780467</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8117809_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8117809: sgZNF397_sgTET2_5hmC_ChIPed_1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP492323">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP492323</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1081832</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20605281">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20605281</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8117809</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8117809</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA were extracted and sheared into fragments with an average size of 200 bp. 60 μg sonicated genomic DNA used in glucose transfer reaction and then proceeded biotinylation reaction. DNA were captured by Dynabeads Myone Streptavidin C1 (Invitrogen™ 65001) and libraries were prepared. Libraries were prepared by using NEBNext1100 ® Ultra™ II DNA Library Prep kit (NEB, E7103) Illuminal NextSeq 2000 P2 100cycles</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23780468" alias="GSM8117810_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23780468</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8117810_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8117810: sgZNF397_sgTET2_5hmC_ChIPed_2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP492323">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP492323</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1081832</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20604538">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20604538</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8117810</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8117810</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA were extracted and sheared into fragments with an average size of 200 bp. 60 μg sonicated genomic DNA used in glucose transfer reaction and then proceeded biotinylation reaction. DNA were captured by Dynabeads Myone Streptavidin C1 (Invitrogen™ 65001) and libraries were prepared. Libraries were prepared by using NEBNext1100 ® Ultra™ II DNA Library Prep kit (NEB, E7103) Illuminal NextSeq 2000 P2 100cycles</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
