SRX3372002 GSM2844016 SRP124659 SRS2669336 GSM2844016 ATAC-seq GENOMIC other cell nuclei were prepared from 50,000 cells, and incubated with 2.5 μl of transposase (Illumina) in a 50-μl reaction for 30 min at 37 °C. ATAC libraries were prepared for sequencing using standard Illumina protocols, After purification of transposase-fragmented DNA, the library was amplified by PCR and subjected to paired-end 50 base-pair high-throughput sequencing on an Illumina HiSeq2500 platform. Illumina HiSeq 2500 gds 302844016 GSM2844016 GEO Accession GSM2844016 SRX3372003 GSM2844017 SRP124659 SRS2669338 GSM2844017 ATAC-seq GENOMIC other cell nuclei were prepared from 50,000 cells, and incubated with 2.5 μl of transposase (Illumina) in a 50-μl reaction for 30 min at 37 °C. ATAC libraries were prepared for sequencing using standard Illumina protocols, After purification of transposase-fragmented DNA, the library was amplified by PCR and subjected to paired-end 50 base-pair high-throughput sequencing on an Illumina HiSeq2500 platform. Illumina HiSeq 2500 gds 302844017 GSM2844017 GEO Accession GSM2844017 SRX3372004 GSM2844018 SRP124659 SRS2669339 GSM2844018 ATAC-seq GENOMIC other cell nuclei were prepared from 50,000 cells, and incubated with 2.5 μl of transposase (Illumina) in a 50-μl reaction for 30 min at 37 °C. ATAC libraries were prepared for sequencing using standard Illumina protocols, After purification of transposase-fragmented DNA, the library was amplified by PCR and subjected to paired-end 50 base-pair high-throughput sequencing on an Illumina HiSeq2500 platform. Illumina HiSeq 2500 gds 302844018 GSM2844018 GEO Accession GSM2844018 SRX3372005 GSM2844019 SRP124659 SRS2669340 GSM2844019 ATAC-seq GENOMIC other cell nuclei were prepared from 50,000 cells, and incubated with 2.5 μl of transposase (Illumina) in a 50-μl reaction for 30 min at 37 °C. ATAC libraries were prepared for sequencing using standard Illumina protocols, After purification of transposase-fragmented DNA, the library was amplified by PCR and subjected to paired-end 50 base-pair high-throughput sequencing on an Illumina HiSeq2500 platform. Illumina HiSeq 2500 gds 302844019 GSM2844019 GEO Accession GSM2844019 SRX3372006 GSM2844020 SRP124659 SRS2669341 GSM2844020 ATAC-seq GENOMIC other cell nuclei were prepared from 50,000 cells, and incubated with 2.5 μl of transposase (Illumina) in a 50-μl reaction for 30 min at 37 °C. ATAC libraries were prepared for sequencing using standard Illumina protocols, After purification of transposase-fragmented DNA, the library was amplified by PCR and subjected to paired-end 50 base-pair high-throughput sequencing on an Illumina HiSeq2500 platform. Illumina HiSeq 2500 gds 302844020 GSM2844020 GEO Accession GSM2844020 SRX3372007 GSM2844021 SRP124659 SRS2669342 GSM2844021 ATAC-seq GENOMIC other cell nuclei were prepared from 50,000 cells, and incubated with 2.5 μl of transposase (Illumina) in a 50-μl reaction for 30 min at 37 °C. ATAC libraries were prepared for sequencing using standard Illumina protocols, After purification of transposase-fragmented DNA, the library was amplified by PCR and subjected to paired-end 50 base-pair high-throughput sequencing on an Illumina HiSeq2500 platform. Illumina HiSeq 2500 gds 302844021 GSM2844021 GEO Accession GSM2844021 SRX3372008 GSM2844022 SRP124659 SRS2669344 GSM2844022 ATAC-seq GENOMIC other cell nuclei were prepared from 50,000 cells, and incubated with 2.5 μl of transposase (Illumina) in a 50-μl reaction for 30 min at 37 °C. ATAC libraries were prepared for sequencing using standard Illumina protocols, After purification of transposase-fragmented DNA, the library was amplified by PCR and subjected to paired-end 50 base-pair high-throughput sequencing on an Illumina HiSeq2500 platform. Illumina HiSeq 2500 gds 302844022 GSM2844022 GEO Accession GSM2844022 SRX3372009 GSM2844023 SRP124659 SRS2669343 GSM2844023 ATAC-seq GENOMIC other cell nuclei were prepared from 50,000 cells, and incubated with 2.5 μl of transposase (Illumina) in a 50-μl reaction for 30 min at 37 °C. ATAC libraries were prepared for sequencing using standard Illumina protocols, After purification of transposase-fragmented DNA, the library was amplified by PCR and subjected to paired-end 50 base-pair high-throughput sequencing on an Illumina HiSeq2500 platform. Illumina HiSeq 2500 gds 302844023 GSM2844023 GEO Accession GSM2844023 SRX3372010 GSM2844024 SRP124659 SRS2669345 GSM2844024 ATAC-seq GENOMIC other cell nuclei were prepared from 50,000 cells, and incubated with 2.5 μl of transposase (Illumina) in a 50-μl reaction for 30 min at 37 °C. ATAC libraries were prepared for sequencing using standard Illumina protocols, After purification of transposase-fragmented DNA, the library was amplified by PCR and subjected to paired-end 50 base-pair high-throughput sequencing on an Illumina HiSeq2500 platform. Illumina HiSeq 2500 gds 302844024 GSM2844024 GEO Accession GSM2844024