SRX18327663 nt1 SRP408933 bp0 Total RNA was poly-A selected and library construction performed with random primers using the Illumina TruSeq Stranded mRNA kit. RNA was fragmented under high temperature with divalent cations. The fragmented RNA was reverse transcribed with random primers. The Illumina library construction was performed with automated liquid handling on the Sciclone instrument (Perkin Elmer). Sequencing on the NovaSeq-6000 was using v. 1.5 chemistry with paired 100-bp reads, reaching 40 milllion reads per library. SRS15816918 Donor1_ctrl nt1 RNA-Seq TRANSCRIPTOMIC PolyA Illumina NovaSeq 6000 SRX18327664 nt2 SRP408933 bp0 Total RNA was poly-A selected and library construction performed with random primers using the Illumina TruSeq Stranded mRNA kit. RNA was fragmented under high temperature with divalent cations. The fragmented RNA was reverse transcribed with random primers. The Illumina library construction was performed with automated liquid handling on the Sciclone instrument (Perkin Elmer). Sequencing on the NovaSeq-6000 was using v. 1.5 chemistry with paired 100-bp reads, reaching 40 milllion reads per library. SRS15816919 Donor2_ctrl nt2 RNA-Seq TRANSCRIPTOMIC PolyA Illumina NovaSeq 6000 SRX18327665 nt3 SRP408933 bp0 Total RNA was poly-A selected and library construction performed with random primers using the Illumina TruSeq Stranded mRNA kit. RNA was fragmented under high temperature with divalent cations. The fragmented RNA was reverse transcribed with random primers. The Illumina library construction was performed with automated liquid handling on the Sciclone instrument (Perkin Elmer). Sequencing on the NovaSeq-6000 was using v. 1.5 chemistry with paired 100-bp reads, reaching 40 milllion reads per library. SRS15816920 Donor3_ctrl nt3 RNA-Seq TRANSCRIPTOMIC PolyA Illumina NovaSeq 6000 SRX18327666 sihtat1 SRP408933 bp0 Total RNA was poly-A selected and library construction performed with random primers using the Illumina TruSeq Stranded mRNA kit. RNA was fragmented under high temperature with divalent cations. The fragmented RNA was reverse transcribed with random primers. The Illumina library construction was performed with automated liquid handling on the Sciclone instrument (Perkin Elmer). Sequencing on the NovaSeq-6000 was using v. 1.5 chemistry with paired 100-bp reads, reaching 40 milllion reads per library. SRS15816921 Donor1_siHTATIP2 sihtat1 RNA-Seq TRANSCRIPTOMIC PolyA Illumina NovaSeq 6000 SRX18327667 sihtat2 SRP408933 bp0 Total RNA was poly-A selected and library construction performed with random primers using the Illumina TruSeq Stranded mRNA kit. RNA was fragmented under high temperature with divalent cations. The fragmented RNA was reverse transcribed with random primers. The Illumina library construction was performed with automated liquid handling on the Sciclone instrument (Perkin Elmer). Sequencing on the NovaSeq-6000 was using v. 1.5 chemistry with paired 100-bp reads, reaching 40 milllion reads per library. SRS15816922 Donor2_siHTATIP2 sihtat2 RNA-Seq TRANSCRIPTOMIC PolyA Illumina NovaSeq 6000 SRX18327668 sihtat3 SRP408933 bp0 Total RNA was poly-A selected and library construction performed with random primers using the Illumina TruSeq Stranded mRNA kit. RNA was fragmented under high temperature with divalent cations. The fragmented RNA was reverse transcribed with random primers. The Illumina library construction was performed with automated liquid handling on the Sciclone instrument (Perkin Elmer). Sequencing on the NovaSeq-6000 was using v. 1.5 chemistry with paired 100-bp reads, reaching 40 milllion reads per library. SRS15816923 Donor3_siHTATIP2 sihtat3 RNA-Seq TRANSCRIPTOMIC PolyA Illumina NovaSeq 6000