SRX2178819 GSM2322597 SRP090169 SRS1704196 GSM2322597 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322597 GEO Accession GSM2322597 SRX2178820 GSM2322598 SRP090169 SRS1704197 GSM2322598 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322598 GEO Accession GSM2322598 SRX2178821 GSM2322599 SRP090169 SRS1704198 GSM2322599 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322599 GEO Accession GSM2322599 SRX2178822 GSM2322600 SRP090169 SRS1704199 GSM2322600 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322600 GEO Accession GSM2322600 SRX2178823 GSM2322601 SRP090169 SRS1704200 GSM2322601 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322601 GEO Accession GSM2322601 SRX2178824 GSM2322602 SRP090169 SRS1704201 GSM2322602 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322602 GEO Accession GSM2322602 SRX2178825 GSM2322603 SRP090169 SRS1704202 GSM2322603 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322603 GEO Accession GSM2322603 SRX2178826 GSM2322604 SRP090169 SRS1704203 GSM2322604 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322604 GEO Accession GSM2322604 SRX2178827 GSM2322605 SRP090169 SRS1704204 GSM2322605 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322605 GEO Accession GSM2322605 SRX2178828 GSM2322606 SRP090169 SRS1704205 GSM2322606 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322606 GEO Accession GSM2322606 SRX2178829 GSM2322607 SRP090169 SRS1704206 GSM2322607 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322607 GEO Accession GSM2322607 SRX2178830 GSM2322608 SRP090169 SRS1704207 GSM2322608 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322608 GEO Accession GSM2322608 SRX2178831 GSM2322609 SRP090169 SRS1704208 GSM2322609 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322609 GEO Accession GSM2322609 SRX2178832 GSM2322610 SRP090169 SRS1704209 GSM2322610 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322610 GEO Accession GSM2322610 SRX2178833 GSM2322611 SRP090169 SRS1704210 GSM2322611 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322611 GEO Accession GSM2322611 SRX2178834 GSM2322612 SRP090169 SRS1704211 GSM2322612 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322612 GEO Accession GSM2322612 SRX2178835 GSM2322613 SRP090169 SRS1704212 GSM2322613 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322613 GEO Accession GSM2322613 SRX2178836 GSM2322614 SRP090169 SRS1704213 GSM2322614 RNA-Seq TRANSCRIPTOMIC cDNA After treatment, cells were resupended in peqGOLD Trifast (VWR International, Germany, cat. no. 30-2010). RNA was extracted according to the manufacturer’s protocol. DNase-I treatment was carried out for 2 hours to eliminate genomic DNA contamination using TURBO DNase kit (Thermo Fisher Scientific cat. No. AM1907). RNA was analyzed by paired end poly(A) RNA sequencing. RNA libraries were prepared using the Illumina TruSeq Stranded mRNA kit. Illumina HiSeq 2000 gds 302322614 GEO Accession GSM2322614