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          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
        </XREF_LINK>
      </SAMPLE_LINK>
    </SAMPLE_LINKS>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>source_name</TAG>
        <VALUE>H9 cells</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>human embryonic stem cells</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>Crispr /Cas9 mediated (HDR) deletion of EXON 2 of NSUN6, clone 2, puromycin selection</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>H9</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRS4249950</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN10741581</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSM3561755</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>H9.KO.2o repl4</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_LINKS>
      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
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    </SAMPLE_LINKS>
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      <SAMPLE_ATTRIBUTE>
        <TAG>source_name</TAG>
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      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>human embryonic stem cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>Crispr /Cas9 mediated (HDR) deletion of EXON 2 of NSUN6, clone 2, puromycin selection</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>H9</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>1</VALUE>
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    </SAMPLE_ATTRIBUTES>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRS4249951</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN10741578</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSM3561756</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>H9.KO.3 repl1</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_LINKS>
      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
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    </SAMPLE_LINKS>
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      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>human embryonic stem cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>Crispr /Cas9 mediated (NHEJ) InDel of exon9 of NSUN6 (deletion of 7nt on allele1 and 50 nt on allele 2 causes framshift and premature stop), clonal</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>H9</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>2</VALUE>
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    </SAMPLE_ATTRIBUTES>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRS4249952</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN10741576</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSM3561758</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>H9.KO.3 repl3</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_LINKS>
      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
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      </SAMPLE_LINK>
    </SAMPLE_LINKS>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>source_name</TAG>
        <VALUE>H9 cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>human embryonic stem cells</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>Crispr /Cas9 mediated (NHEJ) InDel of exon9 of NSUN6 (deletion of 7nt on allele1 and 50 nt on allele 2 causes framshift and premature stop), clonal</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>H9</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>2</VALUE>
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    </SAMPLE_ATTRIBUTES>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRS4249953</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN10741577</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSM3561757</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>H9.KO.3 repl2</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_LINKS>
      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
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      <SAMPLE_ATTRIBUTE>
        <TAG>source_name</TAG>
        <VALUE>H9 cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>human embryonic stem cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>Crispr /Cas9 mediated (NHEJ) InDel of exon9 of NSUN6 (deletion of 7nt on allele1 and 50 nt on allele 2 causes framshift and premature stop), clonal</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>H9</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>2</VALUE>
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    </SAMPLE_ATTRIBUTES>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRS4249954</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN10741580</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSM3561759</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>H9.KO.3 repl4</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_LINKS>
      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
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      <SAMPLE_ATTRIBUTE>
        <TAG>source_name</TAG>
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      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>human embryonic stem cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>Crispr /Cas9 mediated (NHEJ) InDel of exon9 of NSUN6 (deletion of 7nt on allele1 and 50 nt on allele 2 causes framshift and premature stop), clonal</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>H9</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>2</VALUE>
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      <PRIMARY_ID>SRS4249955</PRIMARY_ID>
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    <TITLE>H9.OEX.1 repl1</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
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      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
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        <TAG>cell type</TAG>
        <VALUE>human embryonic stem cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>WT H9 carrying insertions of a piggybac vector coding for a flagged version of NSUN6, puromycin selection, clonal</VALUE>
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        <TAG>cell line</TAG>
        <VALUE>H9</VALUE>
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        <TAG>batch</TAG>
        <VALUE>3</VALUE>
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      <PRIMARY_ID>SRS4249956</PRIMARY_ID>
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    <TITLE>H9.OEX.1 repl2</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
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      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
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        <TAG>cell type</TAG>
        <VALUE>human embryonic stem cells</VALUE>
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        <TAG>genotype/variation</TAG>
        <VALUE>WT H9 carrying insertions of a piggybac vector coding for a flagged version of NSUN6, puromycin selection, clonal</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>H9</VALUE>
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        <TAG>batch</TAG>
        <VALUE>3</VALUE>
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      <PRIMARY_ID>SRS4249957</PRIMARY_ID>
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    <TITLE>H9.OEX.1 repl3</TITLE>
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      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
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          <DB>bioproject</DB>
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        <VALUE>WT H9 carrying insertions of a piggybac vector coding for a flagged version of NSUN6, puromycin selection, clonal</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>source_name</TAG>
        <VALUE>H9 cells</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>human embryonic stem cells</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>WT H9 carrying insertions of a piggybac vector coding for puromycin selection, clone 1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>H9</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>3</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="GSM3561784" accession="SRS4249979">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS4249979</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN10741278</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSM3561784</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>H9.WT.EV2 repl1</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_LINKS>
      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
        </XREF_LINK>
      </SAMPLE_LINK>
    </SAMPLE_LINKS>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>source_name</TAG>
        <VALUE>H9 cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>human embryonic stem cells</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>WT H9 carrying insertions of a piggybac vector coding for puromycin selection, clone 2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>H9</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>3</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRS4249980</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN10741277</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSM3561785</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>H9.WT.EV2 repl2</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
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    <SAMPLE_LINKS>
      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
        </XREF_LINK>
      </SAMPLE_LINK>
    </SAMPLE_LINKS>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>source_name</TAG>
        <VALUE>H9 cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>human embryonic stem cells</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>WT H9 carrying insertions of a piggybac vector coding for puromycin selection, clone 2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>H9</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>3</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRS4249981</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN10741276</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSM3561786</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>H9.WT.EV2 repl3</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_LINKS>
      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
        </XREF_LINK>
      </SAMPLE_LINK>
    </SAMPLE_LINKS>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>source_name</TAG>
        <VALUE>H9 cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>human embryonic stem cells</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>WT H9 carrying insertions of a piggybac vector coding for puromycin selection, clone 2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>H9</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>3</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="GSM3561787" accession="SRS4249982">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS4249982</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN10741275</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSM3561787</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>H9.WT.EV2 repl4</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_LINKS>
      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
        </XREF_LINK>
      </SAMPLE_LINK>
    </SAMPLE_LINKS>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>source_name</TAG>
        <VALUE>H9 cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>human embryonic stem cells</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>WT H9 carrying insertions of a piggybac vector coding for puromycin selection, clone 2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>H9</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>3</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="GSM3561788" accession="SRS4249983">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS4249983</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN10741274</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSM3561788</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>HEK.KO.1 repl1</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_LINKS>
      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
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      </SAMPLE_LINK>
    </SAMPLE_LINKS>
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      <SAMPLE_ATTRIBUTE>
        <TAG>source_name</TAG>
        <VALUE>HEK cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>human embryonic kidney 239 cells</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>Crispr /Cas9 mediated (NHEJ) InDel of exon2 of NSUN6 (deletion causes frameshift and premature stop), clone1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>HEK293</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>4</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRS4249984</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN10741272</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSM3561790</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>HEK.KO.1 repl3</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_LINKS>
      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
        </XREF_LINK>
      </SAMPLE_LINK>
    </SAMPLE_LINKS>
    <SAMPLE_ATTRIBUTES>
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        <TAG>cell type</TAG>
        <VALUE>human embryonic kidney 239 cells</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>Crispr /Cas9 mediated (NHEJ) InDel of exon2 of NSUN6 (deletion causes frameshift and premature stop), clone1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>HEK293</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>4</VALUE>
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    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
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      <PRIMARY_ID>SRS4249985</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN10741273</EXTERNAL_ID>
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    <TITLE>HEK.KO.1 repl2</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
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      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
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        <TAG>cell type</TAG>
        <VALUE>human embryonic kidney 239 cells</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>Crispr /Cas9 mediated (NHEJ) InDel of exon2 of NSUN6 (deletion causes frameshift and premature stop), clone1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>HEK293</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
        <VALUE>4</VALUE>
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    </SAMPLE_ATTRIBUTES>
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      <PRIMARY_ID>SRS4249986</PRIMARY_ID>
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    </IDENTIFIERS>
    <TITLE>HEK.KO.1 repl4</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
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      <SAMPLE_LINK>
        <XREF_LINK>
          <DB>bioproject</DB>
          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
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        <TAG>cell type</TAG>
        <VALUE>human embryonic kidney 239 cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>Crispr /Cas9 mediated (NHEJ) InDel of exon2 of NSUN6 (deletion causes frameshift and premature stop), clone1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
        <VALUE>HEK293</VALUE>
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        <TAG>batch</TAG>
        <VALUE>4</VALUE>
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      <PRIMARY_ID>SRS4249987</PRIMARY_ID>
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    <TITLE>HEK.KO.2 repl1</TITLE>
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      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
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          <DB>bioproject</DB>
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          <LABEL>PRJNA515042</LABEL>
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        <VALUE>human embryonic kidney 239 cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>genotype/variation</TAG>
        <VALUE>Crispr /Cas9 mediated (NHEJ) InDel of exon2 of NSUN6 (deletion causes frameshift and premature stop), clone2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
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        <TAG>batch</TAG>
        <VALUE>4</VALUE>
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      <PRIMARY_ID>SRS4249988</PRIMARY_ID>
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    <TITLE>HEK.KO.2 repl3</TITLE>
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      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
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        <XREF_LINK>
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          <ID>515042</ID>
          <LABEL>PRJNA515042</LABEL>
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      <SAMPLE_ATTRIBUTE>
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        <VALUE>Crispr /Cas9 mediated (NHEJ) InDel of exon2 of NSUN6 (deletion causes frameshift and premature stop), clone2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
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      <SAMPLE_ATTRIBUTE>
        <TAG>batch</TAG>
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      <PRIMARY_ID>SRS4249989</PRIMARY_ID>
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    <TITLE>HEK.KO.2 repl2</TITLE>
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      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
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      <SAMPLE_ATTRIBUTE>
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        <VALUE>Crispr /Cas9 mediated (NHEJ) InDel of exon2 of NSUN6 (deletion causes frameshift and premature stop), clone2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
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        <TAG>batch</TAG>
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    <TITLE>HEK.KO.2 repl4</TITLE>
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      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
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          <LABEL>PRJNA515042</LABEL>
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        <VALUE>human embryonic kidney 239 cells</VALUE>
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      <SAMPLE_ATTRIBUTE>
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        <VALUE>Crispr /Cas9 mediated (NHEJ) InDel of exon2 of NSUN6 (deletion causes frameshift and premature stop), clone2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
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        <TAG>batch</TAG>
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      <PRIMARY_ID>SRS4249991</PRIMARY_ID>
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    <TITLE>HEK.WT.rescue1 repl2</TITLE>
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      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
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      <SAMPLE_ATTRIBUTE>
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      <SAMPLE_ATTRIBUTE>
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      <SAMPLE_ATTRIBUTE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>cell line</TAG>
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