SRX11512737 GSM5464257 SRP329222 SRS9550923 GSM5464257 RNA-Seq TRANSCRIPTOMIC cDNA 50,000 cells were lysed in ATAC lysis buffer and tagmented (Illumina Nextera DNA Library Preparation Kit). After adding SDS, the samples were purified with 2X Agencourt AMPure XP beads (Beckman Coulter A63881) Samples were amplified using NEBNext Q5 Hot Start HiFi PCR Master Mix. The concentration of samples was checked using PicoGreen and median fragment size was checked using the Agilent D1000 screentape on the Agilent Technologies 2200 TapeStation. Samples were sequenced PE50 on a HiSeq 2500. Illumina HiSeq 2500 gds 305464257 GSM5464257 GEO Accession GSM5464257 SRX11512738 GSM5464258 SRP329222 SRS9550924 GSM5464258 RNA-Seq TRANSCRIPTOMIC cDNA 50,000 cells were lysed in ATAC lysis buffer and tagmented (Illumina Nextera DNA Library Preparation Kit). After adding SDS, the samples were purified with 2X Agencourt AMPure XP beads (Beckman Coulter A63881) Samples were amplified using NEBNext Q5 Hot Start HiFi PCR Master Mix. The concentration of samples was checked using PicoGreen and median fragment size was checked using the Agilent D1000 screentape on the Agilent Technologies 2200 TapeStation. Samples were sequenced PE50 on a HiSeq 2500. Illumina HiSeq 2500 gds 305464258 GSM5464258 GEO Accession GSM5464258 SRX11512739 GSM5464259 SRP329222 SRS9550925 GSM5464259 RNA-Seq TRANSCRIPTOMIC cDNA 50,000 cells were lysed in ATAC lysis buffer and tagmented (Illumina Nextera DNA Library Preparation Kit). After adding SDS, the samples were purified with 2X Agencourt AMPure XP beads (Beckman Coulter A63881) Samples were amplified using NEBNext Q5 Hot Start HiFi PCR Master Mix. The concentration of samples was checked using PicoGreen and median fragment size was checked using the Agilent D1000 screentape on the Agilent Technologies 2200 TapeStation. Samples were sequenced PE50 on a HiSeq 2500. Illumina HiSeq 2500 gds 305464259 GSM5464259 GEO Accession GSM5464259 SRX11512740 GSM5464260 SRP329222 SRS9550926 GSM5464260 RNA-Seq TRANSCRIPTOMIC cDNA 50,000 cells were lysed in ATAC lysis buffer and tagmented (Illumina Nextera DNA Library Preparation Kit). After adding SDS, the samples were purified with 2X Agencourt AMPure XP beads (Beckman Coulter A63881) Samples were amplified using NEBNext Q5 Hot Start HiFi PCR Master Mix. The concentration of samples was checked using PicoGreen and median fragment size was checked using the Agilent D1000 screentape on the Agilent Technologies 2200 TapeStation. Samples were sequenced PE50 on a HiSeq 2500. Illumina HiSeq 2500 gds 305464260 GSM5464260 GEO Accession GSM5464260 SRX11512741 GSM5464261 SRP329222 SRS9550927 GSM5464261 RNA-Seq TRANSCRIPTOMIC cDNA 50,000 cells were lysed in ATAC lysis buffer and tagmented (Illumina Nextera DNA Library Preparation Kit). After adding SDS, the samples were purified with 2X Agencourt AMPure XP beads (Beckman Coulter A63881) Samples were amplified using NEBNext Q5 Hot Start HiFi PCR Master Mix. The concentration of samples was checked using PicoGreen and median fragment size was checked using the Agilent D1000 screentape on the Agilent Technologies 2200 TapeStation. Samples were sequenced PE50 on a HiSeq 2500. Illumina HiSeq 2500 gds 305464261 GSM5464261 GEO Accession GSM5464261 SRX11512742 GSM5464262 SRP329222 SRS9550928 GSM5464262 RNA-Seq TRANSCRIPTOMIC cDNA 50,000 cells were lysed in ATAC lysis buffer and tagmented (Illumina Nextera DNA Library Preparation Kit). After adding SDS, the samples were purified with 2X Agencourt AMPure XP beads (Beckman Coulter A63881) Samples were amplified using NEBNext Q5 Hot Start HiFi PCR Master Mix. The concentration of samples was checked using PicoGreen and median fragment size was checked using the Agilent D1000 screentape on the Agilent Technologies 2200 TapeStation. Samples were sequenced PE50 on a HiSeq 2500. Illumina HiSeq 2500 gds 305464262 GSM5464262 GEO Accession GSM5464262 SRX11512743 GSM5464263 SRP329222 SRS9550929 GSM5464263 RNA-Seq TRANSCRIPTOMIC cDNA 50,000 cells were lysed in ATAC lysis buffer and tagmented (Illumina Nextera DNA Library Preparation Kit). After adding SDS, the samples were purified with 2X Agencourt AMPure XP beads (Beckman Coulter A63881) Samples were amplified using NEBNext Q5 Hot Start HiFi PCR Master Mix. The concentration of samples was checked using PicoGreen and median fragment size was checked using the Agilent D1000 screentape on the Agilent Technologies 2200 TapeStation. Samples were sequenced PE50 on a HiSeq 2500. Illumina HiSeq 2500 gds 305464263 GSM5464263 GEO Accession GSM5464263 SRX11512744 GSM5464264 SRP329222 SRS9550930 GSM5464264 RNA-Seq TRANSCRIPTOMIC cDNA 50,000 cells were lysed in ATAC lysis buffer and tagmented (Illumina Nextera DNA Library Preparation Kit). After adding SDS, the samples were purified with 2X Agencourt AMPure XP beads (Beckman Coulter A63881) Samples were amplified using NEBNext Q5 Hot Start HiFi PCR Master Mix. The concentration of samples was checked using PicoGreen and median fragment size was checked using the Agilent D1000 screentape on the Agilent Technologies 2200 TapeStation. Samples were sequenced PE50 on a HiSeq 2500. Illumina HiSeq 2500 gds 305464264 GSM5464264 GEO Accession GSM5464264 SRX11512745 GSM5464265 SRP329222 SRS9550931 GSM5464265 RNA-Seq TRANSCRIPTOMIC cDNA 50,000 cells were lysed in ATAC lysis buffer and tagmented (Illumina Nextera DNA Library Preparation Kit). After adding SDS, the samples were purified with 2X Agencourt AMPure XP beads (Beckman Coulter A63881) Samples were amplified using NEBNext Q5 Hot Start HiFi PCR Master Mix. The concentration of samples was checked using PicoGreen and median fragment size was checked using the Agilent D1000 screentape on the Agilent Technologies 2200 TapeStation. Samples were sequenced PE50 on a HiSeq 2500. Illumina HiSeq 2500 gds 305464265 GSM5464265 GEO Accession GSM5464265 SRX11512746 GSM5464266 SRP329222 SRS9550932 GSM5464266 RNA-Seq TRANSCRIPTOMIC cDNA 50,000 cells were lysed in ATAC lysis buffer and tagmented (Illumina Nextera DNA Library Preparation Kit). After adding SDS, the samples were purified with 2X Agencourt AMPure XP beads (Beckman Coulter A63881) Samples were amplified using NEBNext Q5 Hot Start HiFi PCR Master Mix. The concentration of samples was checked using PicoGreen and median fragment size was checked using the Agilent D1000 screentape on the Agilent Technologies 2200 TapeStation. Samples were sequenced PE50 on a HiSeq 2500. Illumina HiSeq 2500 gds 305464266 GSM5464266 GEO Accession GSM5464266 SRX11512747 GSM5464267 SRP329222 SRS9550933 GSM5464267 RNA-Seq TRANSCRIPTOMIC cDNA 50,000 cells were lysed in ATAC lysis buffer and tagmented (Illumina Nextera DNA Library Preparation Kit). After adding SDS, the samples were purified with 2X Agencourt AMPure XP beads (Beckman Coulter A63881) Samples were amplified using NEBNext Q5 Hot Start HiFi PCR Master Mix. The concentration of samples was checked using PicoGreen and median fragment size was checked using the Agilent D1000 screentape on the Agilent Technologies 2200 TapeStation. Samples were sequenced PE50 on a HiSeq 2500. Illumina HiSeq 2500 gds 305464267 GSM5464267 GEO Accession GSM5464267 SRX11512748 GSM5464268 SRP329222 SRS9550934 GSM5464268 RNA-Seq TRANSCRIPTOMIC cDNA 50,000 cells were lysed in ATAC lysis buffer and tagmented (Illumina Nextera DNA Library Preparation Kit). After adding SDS, the samples were purified with 2X Agencourt AMPure XP beads (Beckman Coulter A63881) Samples were amplified using NEBNext Q5 Hot Start HiFi PCR Master Mix. The concentration of samples was checked using PicoGreen and median fragment size was checked using the Agilent D1000 screentape on the Agilent Technologies 2200 TapeStation. Samples were sequenced PE50 on a HiSeq 2500. Illumina HiSeq 2500 gds 305464268 GSM5464268 GEO Accession GSM5464268