SRX3405131 GSM2860578 SRP125209 SRS2702627 GSM2860578 ATAC-seq GENOMIC other Cell nuclei were fresh prepared from 50,000 cells as previously described (Buenrostro et al. 2013 Nature Methods). ATAC-seq was performed as previously described (Buenrostro et al. 2013 Nature Methods). For each sample, cell nuclei were prepared from 50,000 cells, and incubated with 2.5 uL transposase (Illumina) in a 50 uL reaction for 30 min at 37°C. Following purification of transposase fragmented DNA, the library was amplified by PCR and subjected to high-throughput sequencing using Illumina HiSeq 2500 platform. Illumina HiSeq 2500 gds 302860578 GSM2860578 GEO Accession GSM2860578 SRX3405132 GSM2860579 SRP125209 SRS2702626 GSM2860579 ATAC-seq GENOMIC other Cell nuclei were fresh prepared from 50,000 cells as previously described (Buenrostro et al. 2013 Nature Methods). ATAC-seq was performed as previously described (Buenrostro et al. 2013 Nature Methods). For each sample, cell nuclei were prepared from 50,000 cells, and incubated with 2.5 uL transposase (Illumina) in a 50 uL reaction for 30 min at 37°C. Following purification of transposase fragmented DNA, the library was amplified by PCR and subjected to high-throughput sequencing using Illumina HiSeq 2500 platform. Illumina HiSeq 2500 gds 302860579 GSM2860579 GEO Accession GSM2860579 SRX3405133 GSM2860580 SRP125209 SRS2702630 GSM2860580 ATAC-seq GENOMIC other Cell nuclei were fresh prepared from 50,000 cells as previously described (Buenrostro et al. 2013 Nature Methods). ATAC-seq was performed as previously described (Buenrostro et al. 2013 Nature Methods). For each sample, cell nuclei were prepared from 50,000 cells, and incubated with 2.5 uL transposase (Illumina) in a 50 uL reaction for 30 min at 37°C. Following purification of transposase fragmented DNA, the library was amplified by PCR and subjected to high-throughput sequencing using Illumina HiSeq 2500 platform. Illumina HiSeq 2500 gds 302860580 GSM2860580 GEO Accession GSM2860580 SRX3405134 GSM2860581 SRP125209 SRS2702628 GSM2860581 ATAC-seq GENOMIC other Cell nuclei were fresh prepared from 50,000 cells as previously described (Buenrostro et al. 2013 Nature Methods). ATAC-seq was performed as previously described (Buenrostro et al. 2013 Nature Methods). For each sample, cell nuclei were prepared from 50,000 cells, and incubated with 2.5 uL transposase (Illumina) in a 50 uL reaction for 30 min at 37°C. Following purification of transposase fragmented DNA, the library was amplified by PCR and subjected to high-throughput sequencing using Illumina HiSeq 2500 platform. Illumina HiSeq 2500 gds 302860581 GSM2860581 GEO Accession GSM2860581 SRX3405135 GSM2860582 SRP125209 SRS2702629 GSM2860582 ATAC-seq GENOMIC other Cell nuclei were fresh prepared from 50,000 cells as previously described (Buenrostro et al. 2013 Nature Methods). ATAC-seq was performed as previously described (Buenrostro et al. 2013 Nature Methods). For each sample, cell nuclei were prepared from 50,000 cells, and incubated with 2.5 uL transposase (Illumina) in a 50 uL reaction for 30 min at 37°C. Following purification of transposase fragmented DNA, the library was amplified by PCR and subjected to high-throughput sequencing using Illumina HiSeq 2500 platform. Illumina HiSeq 2500 gds 302860582 GSM2860582 GEO Accession GSM2860582 SRX3405136 GSM2860583 SRP125209 SRS2702631 GSM2860583 ATAC-seq GENOMIC other Cell nuclei were fresh prepared from 50,000 cells as previously described (Buenrostro et al. 2013 Nature Methods). ATAC-seq was performed as previously described (Buenrostro et al. 2013 Nature Methods). For each sample, cell nuclei were prepared from 50,000 cells, and incubated with 2.5 uL transposase (Illumina) in a 50 uL reaction for 30 min at 37°C. Following purification of transposase fragmented DNA, the library was amplified by PCR and subjected to high-throughput sequencing using Illumina HiSeq 2500 platform. Illumina HiSeq 2500 gds 302860583 GSM2860583 GEO Accession GSM2860583 SRX3405137 GSM2860584 SRP125209 SRS2702635 GSM2860584 ATAC-seq GENOMIC other Cell nuclei were fresh prepared from 50,000 cells as previously described (Buenrostro et al. 2013 Nature Methods). ATAC-seq was performed as previously described (Buenrostro et al. 2013 Nature Methods). For each sample, cell nuclei were prepared from 50,000 cells, and incubated with 2.5 uL transposase (Illumina) in a 50 uL reaction for 30 min at 37°C. Following purification of transposase fragmented DNA, the library was amplified by PCR and subjected to high-throughput sequencing using Illumina HiSeq 2500 platform. Illumina HiSeq 2500 gds 302860584 GSM2860584 GEO Accession GSM2860584 SRX3405138 GSM2860585 SRP125209 SRS2702632 GSM2860585 ATAC-seq GENOMIC other Cell nuclei were fresh prepared from 50,000 cells as previously described (Buenrostro et al. 2013 Nature Methods). ATAC-seq was performed as previously described (Buenrostro et al. 2013 Nature Methods). For each sample, cell nuclei were prepared from 50,000 cells, and incubated with 2.5 uL transposase (Illumina) in a 50 uL reaction for 30 min at 37°C. Following purification of transposase fragmented DNA, the library was amplified by PCR and subjected to high-throughput sequencing using Illumina HiSeq 2500 platform. Illumina HiSeq 2500 gds 302860585 GSM2860585 GEO Accession GSM2860585 SRX3405139 GSM2860586 SRP125209 SRS2702633 GSM2860586 ATAC-seq GENOMIC other Cell nuclei were fresh prepared from 50,000 cells as previously described (Buenrostro et al. 2013 Nature Methods). ATAC-seq was performed as previously described (Buenrostro et al. 2013 Nature Methods). For each sample, cell nuclei were prepared from 50,000 cells, and incubated with 2.5 uL transposase (Illumina) in a 50 uL reaction for 30 min at 37°C. Following purification of transposase fragmented DNA, the library was amplified by PCR and subjected to high-throughput sequencing using Illumina HiSeq 2500 platform. Illumina HiSeq 2500 gds 302860586 GSM2860586 GEO Accession GSM2860586 SRX3405140 GSM2860587 SRP125209 SRS2702748 GSM2860587 ATAC-seq GENOMIC other Cell nuclei were fresh prepared from 50,000 cells as previously described (Buenrostro et al. 2013 Nature Methods). ATAC-seq was performed as previously described (Buenrostro et al. 2013 Nature Methods). For each sample, cell nuclei were prepared from 50,000 cells, and incubated with 2.5 uL transposase (Illumina) in a 50 uL reaction for 30 min at 37°C. Following purification of transposase fragmented DNA, the library was amplified by PCR and subjected to high-throughput sequencing using Illumina HiSeq 2500 platform. Illumina HiSeq 2500 gds 302860587 GSM2860587 GEO Accession GSM2860587 SRX3405141 GSM2860588 SRP125209 SRS2702661 GSM2860588 ATAC-seq GENOMIC other Cell nuclei were fresh prepared from 50,000 cells as previously described (Buenrostro et al. 2013 Nature Methods). ATAC-seq was performed as previously described (Buenrostro et al. 2013 Nature Methods). For each sample, cell nuclei were prepared from 50,000 cells, and incubated with 2.5 uL transposase (Illumina) in a 50 uL reaction for 30 min at 37°C. Following purification of transposase fragmented DNA, the library was amplified by PCR and subjected to high-throughput sequencing using Illumina HiSeq 2500 platform. Illumina HiSeq 2500 gds 302860588 GSM2860588 GEO Accession GSM2860588 SRX3405142 GSM2860589 SRP125209 SRS2702665 GSM2860589 ATAC-seq GENOMIC other Cell nuclei were fresh prepared from 50,000 cells as previously described (Buenrostro et al. 2013 Nature Methods). ATAC-seq was performed as previously described (Buenrostro et al. 2013 Nature Methods). For each sample, cell nuclei were prepared from 50,000 cells, and incubated with 2.5 uL transposase (Illumina) in a 50 uL reaction for 30 min at 37°C. Following purification of transposase fragmented DNA, the library was amplified by PCR and subjected to high-throughput sequencing using Illumina HiSeq 2500 platform. Illumina HiSeq 2500 gds 302860589 GSM2860589 GEO Accession GSM2860589