SRX18523828 GSM6797948_r1 SRP411807 PRJNA909596 SRS15991580 GSM6797948 GSM6797948 RNA-Seq TRANSCRIPTOMIC cDNA Cell were washed in PBS, scraped into PBS and pelleted by centrifugation. RNA was isolated from cell pellets using the Monarch Total RNA Miniprep Kit (T2010S, New England Biolabs) including gDNA depletion by gDNA binding columns and on column DNase-1 digest according to the supplier instructions. RNA quality number (RQN) was measured as 10.0 for all samples using an Agilent Fragment Analyzer system. After polyA selection, RNA libraries were prepared for sequencing using the NEBnext ultra II RNA directional kit. Libraries were sequenced on the Illumina NovaSeq 6000 sequencer following the manufacturer's protocols. Illumina NovaSeq 6000 SRX18523829 GSM6797949_r1 SRP411807 PRJNA909596 SRS15991581 GSM6797949 GSM6797949 RNA-Seq TRANSCRIPTOMIC cDNA Cell were washed in PBS, scraped into PBS and pelleted by centrifugation. RNA was isolated from cell pellets using the Monarch Total RNA Miniprep Kit (T2010S, New England Biolabs) including gDNA depletion by gDNA binding columns and on column DNase-1 digest according to the supplier instructions. RNA quality number (RQN) was measured as 10.0 for all samples using an Agilent Fragment Analyzer system. After polyA selection, RNA libraries were prepared for sequencing using the NEBnext ultra II RNA directional kit. Libraries were sequenced on the Illumina NovaSeq 6000 sequencer following the manufacturer's protocols. Illumina NovaSeq 6000 SRX18523830 GSM6797950_r1 SRP411807 PRJNA909596 SRS15991582 GSM6797950 GSM6797950 RNA-Seq TRANSCRIPTOMIC cDNA Cell were washed in PBS, scraped into PBS and pelleted by centrifugation. RNA was isolated from cell pellets using the Monarch Total RNA Miniprep Kit (T2010S, New England Biolabs) including gDNA depletion by gDNA binding columns and on column DNase-1 digest according to the supplier instructions. RNA quality number (RQN) was measured as 10.0 for all samples using an Agilent Fragment Analyzer system. After polyA selection, RNA libraries were prepared for sequencing using the NEBnext ultra II RNA directional kit. Libraries were sequenced on the Illumina NovaSeq 6000 sequencer following the manufacturer's protocols. Illumina NovaSeq 6000 SRX18523831 GSM6797951_r1 SRP411807 PRJNA909596 SRS15991583 GSM6797951 GSM6797951 RNA-Seq TRANSCRIPTOMIC cDNA Cell were washed in PBS, scraped into PBS and pelleted by centrifugation. RNA was isolated from cell pellets using the Monarch Total RNA Miniprep Kit (T2010S, New England Biolabs) including gDNA depletion by gDNA binding columns and on column DNase-1 digest according to the supplier instructions. RNA quality number (RQN) was measured as 10.0 for all samples using an Agilent Fragment Analyzer system. After polyA selection, RNA libraries were prepared for sequencing using the NEBnext ultra II RNA directional kit. Libraries were sequenced on the Illumina NovaSeq 6000 sequencer following the manufacturer's protocols. Illumina NovaSeq 6000 SRX18523832 GSM6797952_r1 SRP411807 PRJNA909596 SRS15991584 GSM6797952 GSM6797952 RNA-Seq TRANSCRIPTOMIC cDNA Cell were washed in PBS, scraped into PBS and pelleted by centrifugation. RNA was isolated from cell pellets using the Monarch Total RNA Miniprep Kit (T2010S, New England Biolabs) including gDNA depletion by gDNA binding columns and on column DNase-1 digest according to the supplier instructions. RNA quality number (RQN) was measured as 10.0 for all samples using an Agilent Fragment Analyzer system. After polyA selection, RNA libraries were prepared for sequencing using the NEBnext ultra II RNA directional kit. Libraries were sequenced on the Illumina NovaSeq 6000 sequencer following the manufacturer's protocols. Illumina NovaSeq 6000 SRX18523833 GSM6797953_r1 SRP411807 PRJNA909596 SRS15991585 GSM6797953 GSM6797953 RNA-Seq TRANSCRIPTOMIC cDNA Cell were washed in PBS, scraped into PBS and pelleted by centrifugation. RNA was isolated from cell pellets using the Monarch Total RNA Miniprep Kit (T2010S, New England Biolabs) including gDNA depletion by gDNA binding columns and on column DNase-1 digest according to the supplier instructions. RNA quality number (RQN) was measured as 10.0 for all samples using an Agilent Fragment Analyzer system. After polyA selection, RNA libraries were prepared for sequencing using the NEBnext ultra II RNA directional kit. Libraries were sequenced on the Illumina NovaSeq 6000 sequencer following the manufacturer's protocols. Illumina NovaSeq 6000 SRX18523834 GSM6797954_r1 SRP411807 PRJNA909596 SRS15991586 GSM6797954 GSM6797954 RNA-Seq TRANSCRIPTOMIC cDNA Cell were washed in PBS, scraped into PBS and pelleted by centrifugation. RNA was isolated from cell pellets using the Monarch Total RNA Miniprep Kit (T2010S, New England Biolabs) including gDNA depletion by gDNA binding columns and on column DNase-1 digest according to the supplier instructions. RNA quality number (RQN) was measured as 10.0 for all samples using an Agilent Fragment Analyzer system. After polyA selection, RNA libraries were prepared for sequencing using the NEBnext ultra II RNA directional kit. Libraries were sequenced on the Illumina NovaSeq 6000 sequencer following the manufacturer's protocols. Illumina NovaSeq 6000 SRX18523835 GSM6797955_r1 SRP411807 PRJNA909596 SRS15991587 GSM6797955 GSM6797955 RNA-Seq TRANSCRIPTOMIC cDNA Cell were washed in PBS, scraped into PBS and pelleted by centrifugation. RNA was isolated from cell pellets using the Monarch Total RNA Miniprep Kit (T2010S, New England Biolabs) including gDNA depletion by gDNA binding columns and on column DNase-1 digest according to the supplier instructions. RNA quality number (RQN) was measured as 10.0 for all samples using an Agilent Fragment Analyzer system. After polyA selection, RNA libraries were prepared for sequencing using the NEBnext ultra II RNA directional kit. Libraries were sequenced on the Illumina NovaSeq 6000 sequencer following the manufacturer's protocols. Illumina NovaSeq 6000