SRX12810937 GSM5660312 SRP343596 SRS10756409 GSM5660312 ATAC-seq GENOMIC other Cells were washed in PBS twice, counted and nuclei were isolated from 100,000 cells using 100 μl hypotonic buffer (10 mM Tris pH 7.4, 10 mM NaCl, 3 mM MgCl2, 0.1% NP40) to generate two independent transposition reactions. Nuclei were split in half and treated with 2.5 μl Illumina Tn5 Transposase for 30 min at 37 °C. DNA were isolated from transposed nuclei. The libraries were constructed by PCR using barcoded Illumina Nextera primers. Illumina HiSeq 2500 gds 305660312 GSM5660312 GEO Accession GSM5660312 SRX12810938 GSM5660313 SRP343596 SRS10756410 GSM5660313 ATAC-seq GENOMIC other Cells were washed in PBS twice, counted and nuclei were isolated from 100,000 cells using 100 μl hypotonic buffer (10 mM Tris pH 7.4, 10 mM NaCl, 3 mM MgCl2, 0.1% NP40) to generate two independent transposition reactions. Nuclei were split in half and treated with 2.5 μl Illumina Tn5 Transposase for 30 min at 37 °C. DNA were isolated from transposed nuclei. The libraries were constructed by PCR using barcoded Illumina Nextera primers. Illumina HiSeq 2500 gds 305660313 GSM5660313 GEO Accession GSM5660313 SRX12810939 GSM5660314 SRP343596 SRS10756411 GSM5660314 ATAC-seq GENOMIC other Cells were washed in PBS twice, counted and nuclei were isolated from 100,000 cells using 100 μl hypotonic buffer (10 mM Tris pH 7.4, 10 mM NaCl, 3 mM MgCl2, 0.1% NP40) to generate two independent transposition reactions. Nuclei were split in half and treated with 2.5 μl Illumina Tn5 Transposase for 30 min at 37 °C. DNA were isolated from transposed nuclei. The libraries were constructed by PCR using barcoded Illumina Nextera primers. Illumina HiSeq 2500 gds 305660314 GSM5660314 GEO Accession GSM5660314 SRX12810940 GSM5660315 SRP343596 SRS10756412 GSM5660315 ATAC-seq GENOMIC other Cells were washed in PBS twice, counted and nuclei were isolated from 100,000 cells using 100 μl hypotonic buffer (10 mM Tris pH 7.4, 10 mM NaCl, 3 mM MgCl2, 0.1% NP40) to generate two independent transposition reactions. Nuclei were split in half and treated with 2.5 μl Illumina Tn5 Transposase for 30 min at 37 °C. DNA were isolated from transposed nuclei. The libraries were constructed by PCR using barcoded Illumina Nextera primers. Illumina HiSeq 2500 gds 305660315 GSM5660315 GEO Accession GSM5660315 SRX12810941 GSM5660316 SRP343596 SRS10756413 GSM5660316 ATAC-seq GENOMIC other Cells were washed in PBS twice, counted and nuclei were isolated from 100,000 cells using 100 μl hypotonic buffer (10 mM Tris pH 7.4, 10 mM NaCl, 3 mM MgCl2, 0.1% NP40) to generate two independent transposition reactions. Nuclei were split in half and treated with 2.5 μl Illumina Tn5 Transposase for 30 min at 37 °C. DNA were isolated from transposed nuclei. The libraries were constructed by PCR using barcoded Illumina Nextera primers. Illumina HiSeq 2500 gds 305660316 GSM5660316 GEO Accession GSM5660316 SRX12810942 GSM5660317 SRP343596 SRS10756414 GSM5660317 ATAC-seq GENOMIC other Cells were washed in PBS twice, counted and nuclei were isolated from 100,000 cells using 100 μl hypotonic buffer (10 mM Tris pH 7.4, 10 mM NaCl, 3 mM MgCl2, 0.1% NP40) to generate two independent transposition reactions. Nuclei were split in half and treated with 2.5 μl Illumina Tn5 Transposase for 30 min at 37 °C. DNA were isolated from transposed nuclei. The libraries were constructed by PCR using barcoded Illumina Nextera primers. Illumina HiSeq 2500 gds 305660317 GSM5660317 GEO Accession GSM5660317