SRX15183765 GSM6111858_r1 SRP373914 PRJNA835696 SRS12924128 GSM6111858 GSM6111858 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA quality was assessed using the TapeStation 2200 (Agilent). At least 1ng of DNase-treated total was used to generate indexed mRNA libraries using SMART-Seq Ultra Low Input RNA-seq V3 kits (Takara). Library quality was assessed using the TapeStation 2200 (Agilent) and libraries were quantitated using KAPA Library Quantification Kits (Roche). Pooled libraries were subjected to 50 bp single-end sequencing according to the manufacturer's protocol (Illumina HiSeq2500). Illumina HiSeq 2500 SRX15183766 GSM6111859_r1 SRP373914 PRJNA835696 SRS12924129 GSM6111859 GSM6111859 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA quality was assessed using the TapeStation 2200 (Agilent). At least 1ng of DNase-treated total was used to generate indexed mRNA libraries using SMART-Seq Ultra Low Input RNA-seq V3 kits (Takara). Library quality was assessed using the TapeStation 2200 (Agilent) and libraries were quantitated using KAPA Library Quantification Kits (Roche). Pooled libraries were subjected to 50 bp single-end sequencing according to the manufacturer's protocol (Illumina HiSeq2500). Illumina HiSeq 2500 SRX15183767 GSM6111860_r1 SRP373914 PRJNA835696 SRS12924127 GSM6111860 GSM6111860 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA quality was assessed using the TapeStation 2200 (Agilent). At least 1ng of DNase-treated total was used to generate indexed mRNA libraries using SMART-Seq Ultra Low Input RNA-seq V3 kits (Takara). Library quality was assessed using the TapeStation 2200 (Agilent) and libraries were quantitated using KAPA Library Quantification Kits (Roche). Pooled libraries were subjected to 50 bp single-end sequencing according to the manufacturer's protocol (Illumina HiSeq2500). Illumina HiSeq 2500 SRX15183768 GSM6111861_r1 SRP373914 PRJNA835696 SRS12924130 GSM6111861 GSM6111861 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA quality was assessed using the TapeStation 2200 (Agilent). At least 1ng of DNase-treated total was used to generate indexed mRNA libraries using SMART-Seq Ultra Low Input RNA-seq V3 kits (Takara). Library quality was assessed using the TapeStation 2200 (Agilent) and libraries were quantitated using KAPA Library Quantification Kits (Roche). Pooled libraries were subjected to 50 bp single-end sequencing according to the manufacturer's protocol (Illumina HiSeq2500). Illumina HiSeq 2500 SRX15183769 GSM6111862_r1 SRP373914 PRJNA835696 SRS12924131 GSM6111862 GSM6111862 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA quality was assessed using the TapeStation 2200 (Agilent). At least 1ng of DNase-treated total was used to generate indexed mRNA libraries using SMART-Seq Ultra Low Input RNA-seq V3 kits (Takara). Library quality was assessed using the TapeStation 2200 (Agilent) and libraries were quantitated using KAPA Library Quantification Kits (Roche). Pooled libraries were subjected to 50 bp single-end sequencing according to the manufacturer's protocol (Illumina HiSeq2500). Illumina HiSeq 2500 SRX15183770 GSM6111863_r1 SRP373914 PRJNA835696 SRS12924133 GSM6111863 GSM6111863 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA quality was assessed using the TapeStation 2200 (Agilent). At least 1ng of DNase-treated total was used to generate indexed mRNA libraries using SMART-Seq Ultra Low Input RNA-seq V3 kits (Takara). Library quality was assessed using the TapeStation 2200 (Agilent) and libraries were quantitated using KAPA Library Quantification Kits (Roche). Pooled libraries were subjected to 50 bp single-end sequencing according to the manufacturer's protocol (Illumina HiSeq2500). Illumina HiSeq 2500