SRX18009979 GSM6674703_r1 SRP404313 PRJNA893685 SRS15518725 GSM6674703 GSM6674703 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009980 GSM6674702_r1 SRP404313 PRJNA893685 SRS15518726 GSM6674702 GSM6674702 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009981 GSM6674701_r1 SRP404313 PRJNA893685 SRS15518727 GSM6674701 GSM6674701 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009982 GSM6674700_r1 SRP404313 PRJNA893685 SRS15518728 GSM6674700 GSM6674700 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009983 GSM6674699_r1 SRP404313 PRJNA893685 SRS15518729 GSM6674699 GSM6674699 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009984 GSM6674710_r1 SRP404313 PRJNA893685 SRS15518730 GSM6674710 GSM6674710 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009985 GSM6674709_r1 SRP404313 PRJNA893685 SRS15518731 GSM6674709 GSM6674709 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009986 GSM6674708_r1 SRP404313 PRJNA893685 SRS15518732 GSM6674708 GSM6674708 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009987 GSM6674707_r1 SRP404313 PRJNA893685 SRS15518733 GSM6674707 GSM6674707 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009988 GSM6674706_r1 SRP404313 PRJNA893685 SRS15518735 GSM6674706 GSM6674706 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009989 GSM6674705_r1 SRP404313 PRJNA893685 SRS15518734 GSM6674705 GSM6674705 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009990 GSM6674704_r1 SRP404313 PRJNA893685 SRS15518736 GSM6674704 GSM6674704 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009991 GSM6674711_r1 SRP404313 PRJNA893685 SRS15518737 GSM6674711 GSM6674711 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009992 GSM6674712_r1 SRP404313 PRJNA893685 SRS15518738 GSM6674712 GSM6674712 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009993 GSM6674713_r1 SRP404313 PRJNA893685 SRS15518739 GSM6674713 GSM6674713 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009994 GSM6674716_r1 SRP404313 PRJNA893685 SRS15518740 GSM6674716 GSM6674716 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009995 GSM6674717_r1 SRP404313 PRJNA893685 SRS15518741 GSM6674717 GSM6674717 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009996 GSM6674718_r1 SRP404313 PRJNA893685 SRS15518742 GSM6674718 GSM6674718 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009997 GSM6674719_r1 SRP404313 PRJNA893685 SRS15518743 GSM6674719 GSM6674719 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009998 GSM6674720_r1 SRP404313 PRJNA893685 SRS15518744 GSM6674720 GSM6674720 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18009999 GSM6674721_r1 SRP404313 PRJNA893685 SRS15518745 GSM6674721 GSM6674721 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010000 GSM6674722_r1 SRP404313 PRJNA893685 SRS15518746 GSM6674722 GSM6674722 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010001 GSM6674723_r1 SRP404313 PRJNA893685 SRS15518747 GSM6674723 GSM6674723 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010002 GSM6674714_r1 SRP404313 PRJNA893685 SRS15518748 GSM6674714 GSM6674714 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010003 GSM6674715_r1 SRP404313 PRJNA893685 SRS15518749 GSM6674715 GSM6674715 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010004 GSM6674726_r1 SRP404313 PRJNA893685 SRS15518751 GSM6674726 GSM6674726 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010005 GSM6674727_r1 SRP404313 PRJNA893685 SRS15518750 GSM6674727 GSM6674727 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010006 GSM6674728_r1 SRP404313 PRJNA893685 SRS15518752 GSM6674728 GSM6674728 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010007 GSM6674729_r1 SRP404313 PRJNA893685 SRS15518753 GSM6674729 GSM6674729 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010008 GSM6674730_r1 SRP404313 PRJNA893685 SRS15518754 GSM6674730 GSM6674730 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010009 GSM6674731_r1 SRP404313 PRJNA893685 SRS15518755 GSM6674731 GSM6674731 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010010 GSM6674732_r1 SRP404313 PRJNA893685 SRS15518756 GSM6674732 GSM6674732 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010011 GSM6674733_r1 SRP404313 PRJNA893685 SRS15518757 GSM6674733 GSM6674733 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010012 GSM6674724_r1 SRP404313 PRJNA893685 SRS15518758 GSM6674724 GSM6674724 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010013 GSM6674725_r1 SRP404313 PRJNA893685 SRS15518759 GSM6674725 GSM6674725 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010014 GSM6674734_r1 SRP404313 PRJNA893685 SRS15518760 GSM6674734 GSM6674734 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010015 GSM6674737_r1 SRP404313 PRJNA893685 SRS15518761 GSM6674737 GSM6674737 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010016 GSM6674738_r1 SRP404313 PRJNA893685 SRS15518762 GSM6674738 GSM6674738 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010017 GSM6674739_r1 SRP404313 PRJNA893685 SRS15518763 GSM6674739 GSM6674739 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010018 GSM6674740_r1 SRP404313 PRJNA893685 SRS15518764 GSM6674740 GSM6674740 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010019 GSM6674741_r1 SRP404313 PRJNA893685 SRS15518766 GSM6674741 GSM6674741 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010020 GSM6674742_r1 SRP404313 PRJNA893685 SRS15518765 GSM6674742 GSM6674742 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010021 GSM6674743_r1 SRP404313 PRJNA893685 SRS15518767 GSM6674743 GSM6674743 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010022 GSM6674744_r1 SRP404313 PRJNA893685 SRS15518768 GSM6674744 GSM6674744 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010023 GSM6674745_r1 SRP404313 PRJNA893685 SRS15518769 GSM6674745 GSM6674745 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010024 GSM6674735_r1 SRP404313 PRJNA893685 SRS15518770 GSM6674735 GSM6674735 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010025 GSM6674736_r1 SRP404313 PRJNA893685 SRS15518771 GSM6674736 GSM6674736 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010026 GSM6674747_r1 SRP404313 PRJNA893685 SRS15518772 GSM6674747 GSM6674747 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010027 GSM6674748_r1 SRP404313 PRJNA893685 SRS15518773 GSM6674748 GSM6674748 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010028 GSM6674749_r1 SRP404313 PRJNA893685 SRS15518774 GSM6674749 GSM6674749 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010029 GSM6674750_r1 SRP404313 PRJNA893685 SRS15518775 GSM6674750 GSM6674750 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010030 GSM6674751_r1 SRP404313 PRJNA893685 SRS15518776 GSM6674751 GSM6674751 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000 SRX18010031 GSM6674746_r1 SRP404313 PRJNA893685 SRS15518777 GSM6674746 GSM6674746 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from cells using the Nucleospin® (Macherey-Nagel, USA) kit. Total RNA was quantified using Qubit fluorometer (Thermo Fisher Scientific, USA) and quality controlled on an Agilent Tapestation (Agilent, Santa Clara, USA). RNA-seq libraries were prepared using the Ribo-Zero Plus rRNA Depletion kit (Illumina) followed by TruSeq Stranded Total RNA kit (Illumina) at the IGM Genomics Center at UC San Diego. Libraries were pooled and sequenced on NovaSeq 6000 S1 Flow Cell (Illumina) to an average depth of 23 million uniquely mapped reads. Illumina NovaSeq 6000