SRX11242575 GSM5403566 SRP325825 SRS9286547 GSM5403566 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403566 GSM5403566 GEO Accession GSM5403566 SRX11242576 GSM5403567 SRP325825 SRS9286548 GSM5403567 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403567 GSM5403567 GEO Accession GSM5403567 SRX11242577 GSM5403568 SRP325825 SRS9286549 GSM5403568 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403568 GSM5403568 GEO Accession GSM5403568 SRX11242578 GSM5403569 SRP325825 SRS9286550 GSM5403569 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403569 GSM5403569 GEO Accession GSM5403569 SRX11242579 GSM5403570 SRP325825 SRS9286551 GSM5403570 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403570 GSM5403570 GEO Accession GSM5403570 SRX11242580 GSM5403571 SRP325825 SRS9286552 GSM5403571 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403571 GSM5403571 GEO Accession GSM5403571 SRX11242581 GSM5403572 SRP325825 SRS9286553 GSM5403572 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403572 GSM5403572 GEO Accession GSM5403572 SRX11242582 GSM5403573 SRP325825 SRS9286554 GSM5403573 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403573 GSM5403573 GEO Accession GSM5403573 SRX11242583 GSM5403574 SRP325825 SRS9286555 GSM5403574 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403574 GSM5403574 GEO Accession GSM5403574 SRX11242584 GSM5403575 SRP325825 SRS9286556 GSM5403575 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403575 GSM5403575 GEO Accession GSM5403575 SRX11242585 GSM5403576 SRP325825 SRS9286557 GSM5403576 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403576 GSM5403576 GEO Accession GSM5403576 SRX11242586 GSM5403577 SRP325825 SRS9286558 GSM5403577 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403577 GSM5403577 GEO Accession GSM5403577 SRX11242587 GSM5403578 SRP325825 SRS9286559 GSM5403578 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403578 GSM5403578 GEO Accession GSM5403578 SRX11242588 GSM5403579 SRP325825 SRS9286560 GSM5403579 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403579 GSM5403579 GEO Accession GSM5403579 SRX11242589 GSM5403580 SRP325825 SRS9286561 GSM5403580 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403580 GSM5403580 GEO Accession GSM5403580 SRX11242590 GSM5403581 SRP325825 SRS9286562 GSM5403581 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403581 GSM5403581 GEO Accession GSM5403581 SRX11242591 GSM5403582 SRP325825 SRS9286563 GSM5403582 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403582 GSM5403582 GEO Accession GSM5403582 SRX11242592 GSM5403583 SRP325825 SRS9286564 GSM5403583 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403583 GSM5403583 GEO Accession GSM5403583 SRX11242593 GSM5403584 SRP325825 SRS9286565 GSM5403584 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403584 GSM5403584 GEO Accession GSM5403584 SRX11242594 GSM5403585 SRP325825 SRS9286566 GSM5403585 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403585 GSM5403585 GEO Accession GSM5403585 SRX11242595 GSM5403586 SRP325825 SRS9286567 GSM5403586 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403586 GSM5403586 GEO Accession GSM5403586 SRX11242596 GSM5403587 SRP325825 SRS9286568 GSM5403587 ATAC-seq GENOMIC other Fifty thousand cells were collected and centrifuged. The cells were lysed to collect the nuclei, which were broken down with transposase. Fragmented product was purified by VAHTS DNA Clean Beads. After purification, the DNAs was PCR-amplified and purified by VAHTS DNA Clean Beads. High- throughput sequencing was performed using Illumina HiSeq Xten (Illumina) platform with PE150 (pair-end sequencing, 150 bp reads). Illumina NovaSeq 6000 gds 305403587 GSM5403587 GEO Accession GSM5403587