SRX18327461 GSM6745321_r1 SRP408927 PRJNA903848 SRS15816717 GSM6745321 GSM6745321 ATAC-seq GENOMIC other A previously published OMNI ATAC-Seq protocol (Corces et al, 2017) was used for cell lysis, tagmentation, and DNA purification. The Tn5 treated DNA was amplified with 10 cycles of PCR in 50 μl reaction volumes. 1.8X AmpurXP beads purification was used for the PCR product clean-up. The libraries were validated with Agilent Bioanalyzer DNA High Sensitivity Kit, and quantified with qPCR. ATAC-seq libraries were sequenced on Illumina NovaSeq6000 with S4 Reagent v1.5 kit (Illumina, Cat 20028312) at Tgen with the sequencing length of 2x101. Real-time analysis (RTA) 3.4.4 software was used to process the image analysis. Illumina NovaSeq 6000 SRX18327462 GSM6745322_r1 SRP408927 PRJNA903848 SRS15816718 GSM6745322 GSM6745322 ATAC-seq GENOMIC other A previously published OMNI ATAC-Seq protocol (Corces et al, 2017) was used for cell lysis, tagmentation, and DNA purification. The Tn5 treated DNA was amplified with 10 cycles of PCR in 50 μl reaction volumes. 1.8X AmpurXP beads purification was used for the PCR product clean-up. The libraries were validated with Agilent Bioanalyzer DNA High Sensitivity Kit, and quantified with qPCR. ATAC-seq libraries were sequenced on Illumina NovaSeq6000 with S4 Reagent v1.5 kit (Illumina, Cat 20028312) at Tgen with the sequencing length of 2x101. Real-time analysis (RTA) 3.4.4 software was used to process the image analysis. Illumina NovaSeq 6000 SRX18327463 GSM6745323_r1 SRP408927 PRJNA903848 SRS15816719 GSM6745323 GSM6745323 ATAC-seq GENOMIC other A previously published OMNI ATAC-Seq protocol (Corces et al, 2017) was used for cell lysis, tagmentation, and DNA purification. The Tn5 treated DNA was amplified with 10 cycles of PCR in 50 μl reaction volumes. 1.8X AmpurXP beads purification was used for the PCR product clean-up. The libraries were validated with Agilent Bioanalyzer DNA High Sensitivity Kit, and quantified with qPCR. ATAC-seq libraries were sequenced on Illumina NovaSeq6000 with S4 Reagent v1.5 kit (Illumina, Cat 20028312) at Tgen with the sequencing length of 2x101. Real-time analysis (RTA) 3.4.4 software was used to process the image analysis. Illumina NovaSeq 6000 SRX18327464 GSM6745324_r1 SRP408927 PRJNA903848 SRS15816720 GSM6745324 GSM6745324 ATAC-seq GENOMIC other A previously published OMNI ATAC-Seq protocol (Corces et al, 2017) was used for cell lysis, tagmentation, and DNA purification. The Tn5 treated DNA was amplified with 10 cycles of PCR in 50 μl reaction volumes. 1.8X AmpurXP beads purification was used for the PCR product clean-up. The libraries were validated with Agilent Bioanalyzer DNA High Sensitivity Kit, and quantified with qPCR. ATAC-seq libraries were sequenced on Illumina NovaSeq6000 with S4 Reagent v1.5 kit (Illumina, Cat 20028312) at Tgen with the sequencing length of 2x101. Real-time analysis (RTA) 3.4.4 software was used to process the image analysis. Illumina NovaSeq 6000 SRX18327465 GSM6745325_r1 SRP408927 PRJNA903848 SRS15816721 GSM6745325 GSM6745325 ATAC-seq GENOMIC other A previously published OMNI ATAC-Seq protocol (Corces et al, 2017) was used for cell lysis, tagmentation, and DNA purification. The Tn5 treated DNA was amplified with 10 cycles of PCR in 50 μl reaction volumes. 1.8X AmpurXP beads purification was used for the PCR product clean-up. The libraries were validated with Agilent Bioanalyzer DNA High Sensitivity Kit, and quantified with qPCR. ATAC-seq libraries were sequenced on Illumina NovaSeq6000 with S4 Reagent v1.5 kit (Illumina, Cat 20028312) at Tgen with the sequencing length of 2x101. Real-time analysis (RTA) 3.4.4 software was used to process the image analysis. Illumina NovaSeq 6000 SRX18327466 GSM6745326_r1 SRP408927 PRJNA903848 SRS15816722 GSM6745326 GSM6745326 ATAC-seq GENOMIC other A previously published OMNI ATAC-Seq protocol (Corces et al, 2017) was used for cell lysis, tagmentation, and DNA purification. The Tn5 treated DNA was amplified with 10 cycles of PCR in 50 μl reaction volumes. 1.8X AmpurXP beads purification was used for the PCR product clean-up. The libraries were validated with Agilent Bioanalyzer DNA High Sensitivity Kit, and quantified with qPCR. ATAC-seq libraries were sequenced on Illumina NovaSeq6000 with S4 Reagent v1.5 kit (Illumina, Cat 20028312) at Tgen with the sequencing length of 2x101. Real-time analysis (RTA) 3.4.4 software was used to process the image analysis. Illumina NovaSeq 6000 SRX18327467 GSM6745327_r1 SRP408927 PRJNA903848 SRS15816723 GSM6745327 GSM6745327 ATAC-seq GENOMIC other A previously published OMNI ATAC-Seq protocol (Corces et al, 2017) was used for cell lysis, tagmentation, and DNA purification. The Tn5 treated DNA was amplified with 10 cycles of PCR in 50 μl reaction volumes. 1.8X AmpurXP beads purification was used for the PCR product clean-up. The libraries were validated with Agilent Bioanalyzer DNA High Sensitivity Kit, and quantified with qPCR. ATAC-seq libraries were sequenced on Illumina NovaSeq6000 with S4 Reagent v1.5 kit (Illumina, Cat 20028312) at Tgen with the sequencing length of 2x101. Real-time analysis (RTA) 3.4.4 software was used to process the image analysis. Illumina NovaSeq 6000 SRX18327468 GSM6745328_r1 SRP408927 PRJNA903848 SRS15816724 GSM6745328 GSM6745328 ATAC-seq GENOMIC other A previously published OMNI ATAC-Seq protocol (Corces et al, 2017) was used for cell lysis, tagmentation, and DNA purification. The Tn5 treated DNA was amplified with 10 cycles of PCR in 50 μl reaction volumes. 1.8X AmpurXP beads purification was used for the PCR product clean-up. The libraries were validated with Agilent Bioanalyzer DNA High Sensitivity Kit, and quantified with qPCR. ATAC-seq libraries were sequenced on Illumina NovaSeq6000 with S4 Reagent v1.5 kit (Illumina, Cat 20028312) at Tgen with the sequencing length of 2x101. Real-time analysis (RTA) 3.4.4 software was used to process the image analysis. Illumina NovaSeq 6000 SRX18327469 GSM6745329_r1 SRP408927 PRJNA903848 SRS15816725 GSM6745329 GSM6745329 ATAC-seq GENOMIC other A previously published OMNI ATAC-Seq protocol (Corces et al, 2017) was used for cell lysis, tagmentation, and DNA purification. The Tn5 treated DNA was amplified with 10 cycles of PCR in 50 μl reaction volumes. 1.8X AmpurXP beads purification was used for the PCR product clean-up. The libraries were validated with Agilent Bioanalyzer DNA High Sensitivity Kit, and quantified with qPCR. ATAC-seq libraries were sequenced on Illumina NovaSeq6000 with S4 Reagent v1.5 kit (Illumina, Cat 20028312) at Tgen with the sequencing length of 2x101. Real-time analysis (RTA) 3.4.4 software was used to process the image analysis. Illumina NovaSeq 6000 SRX18327470 GSM6745330_r1 SRP408927 PRJNA903848 SRS15816726 GSM6745330 GSM6745330 ATAC-seq GENOMIC other A previously published OMNI ATAC-Seq protocol (Corces et al, 2017) was used for cell lysis, tagmentation, and DNA purification. The Tn5 treated DNA was amplified with 10 cycles of PCR in 50 μl reaction volumes. 1.8X AmpurXP beads purification was used for the PCR product clean-up. The libraries were validated with Agilent Bioanalyzer DNA High Sensitivity Kit, and quantified with qPCR. ATAC-seq libraries were sequenced on Illumina NovaSeq6000 with S4 Reagent v1.5 kit (Illumina, Cat 20028312) at Tgen with the sequencing length of 2x101. Real-time analysis (RTA) 3.4.4 software was used to process the image analysis. Illumina NovaSeq 6000 SRX18327471 GSM6745331_r1 SRP408927 PRJNA903848 SRS15816727 GSM6745331 GSM6745331 ATAC-seq GENOMIC other A previously published OMNI ATAC-Seq protocol (Corces et al, 2017) was used for cell lysis, tagmentation, and DNA purification. The Tn5 treated DNA was amplified with 10 cycles of PCR in 50 μl reaction volumes. 1.8X AmpurXP beads purification was used for the PCR product clean-up. The libraries were validated with Agilent Bioanalyzer DNA High Sensitivity Kit, and quantified with qPCR. ATAC-seq libraries were sequenced on Illumina NovaSeq6000 with S4 Reagent v1.5 kit (Illumina, Cat 20028312) at Tgen with the sequencing length of 2x101. Real-time analysis (RTA) 3.4.4 software was used to process the image analysis. Illumina NovaSeq 6000 SRX18327472 GSM6745332_r1 SRP408927 PRJNA903848 SRS15816728 GSM6745332 GSM6745332 ATAC-seq GENOMIC other A previously published OMNI ATAC-Seq protocol (Corces et al, 2017) was used for cell lysis, tagmentation, and DNA purification. The Tn5 treated DNA was amplified with 10 cycles of PCR in 50 μl reaction volumes. 1.8X AmpurXP beads purification was used for the PCR product clean-up. The libraries were validated with Agilent Bioanalyzer DNA High Sensitivity Kit, and quantified with qPCR. ATAC-seq libraries were sequenced on Illumina NovaSeq6000 with S4 Reagent v1.5 kit (Illumina, Cat 20028312) at Tgen with the sequencing length of 2x101. Real-time analysis (RTA) 3.4.4 software was used to process the image analysis. Illumina NovaSeq 6000