<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE124223" accession="SRP174122">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP174122</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA511015</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE124223</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Chromatin accesibility in human DP3 thymocytes and T-ALL tumors</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>Long-range enhancers play an important role in the temporal and spatial control of gene expression and are deregulated in many cancers. Yet, the mechanisms that govern enhancer activity during development and oncogenesis remain poorly understood. In this study we analyze the chromatin accesibility of DP3 minus cells and three human T-ALL leukemia. Overall design: ATAC-seq sample from DP3 minus cells and three human T-ALL leukemia.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE124223</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
