SRX3506666 GSM2901301 SRP127468 SRS2784213 GSM2901301 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901301 GSM2901301 GEO Accession GSM2901301 SRX3506667 GSM2901302 SRP127468 SRS2784214 GSM2901302 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901302 GSM2901302 GEO Accession GSM2901302 SRX3506668 GSM2901303 SRP127468 SRS2784228 GSM2901303 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901303 GSM2901303 GEO Accession GSM2901303 SRX3506669 GSM2901304 SRP127468 SRS2784215 GSM2901304 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901304 GSM2901304 GEO Accession GSM2901304 SRX3506670 GSM2901305 SRP127468 SRS2784216 GSM2901305 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901305 GSM2901305 GEO Accession GSM2901305 SRX3506671 GSM2901306 SRP127468 SRS2784217 GSM2901306 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901306 GSM2901306 GEO Accession GSM2901306 SRX3506672 GSM2901307 SRP127468 SRS2784218 GSM2901307 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901307 GSM2901307 GEO Accession GSM2901307 SRX3506673 GSM2901308 SRP127468 SRS2784219 GSM2901308 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901308 GSM2901308 GEO Accession GSM2901308 SRX3506674 GSM2901309 SRP127468 SRS2784220 GSM2901309 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901309 GSM2901309 GEO Accession GSM2901309 SRX3506675 GSM2901310 SRP127468 SRS2784224 GSM2901310 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901310 GSM2901310 GEO Accession GSM2901310 SRX3506676 GSM2901311 SRP127468 SRS2784221 GSM2901311 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901311 GSM2901311 GEO Accession GSM2901311 SRX3506677 GSM2901312 SRP127468 SRS2784236 GSM2901312 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901312 GSM2901312 GEO Accession GSM2901312 SRX3506678 GSM2901313 SRP127468 SRS2784226 GSM2901313 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901313 GSM2901313 GEO Accession GSM2901313 SRX3506679 GSM2901314 SRP127468 SRS2784222 GSM2901314 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901314 GSM2901314 GEO Accession GSM2901314 SRX3506680 GSM2901315 SRP127468 SRS2784223 GSM2901315 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901315 GSM2901315 GEO Accession GSM2901315 SRX3506681 GSM2901316 SRP127468 SRS2784237 GSM2901316 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901316 GSM2901316 GEO Accession GSM2901316 SRX3506682 GSM2901317 SRP127468 SRS2784225 GSM2901317 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901317 GSM2901317 GEO Accession GSM2901317 SRX3506683 GSM2901318 SRP127468 SRS2784235 GSM2901318 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901318 GSM2901318 GEO Accession GSM2901318 SRX3506684 GSM2901319 SRP127468 SRS2784227 GSM2901319 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901319 GSM2901319 GEO Accession GSM2901319 SRX3506685 GSM2901320 SRP127468 SRS2784238 GSM2901320 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901320 GSM2901320 GEO Accession GSM2901320 SRX3506686 GSM2901321 SRP127468 SRS2784229 GSM2901321 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901321 GSM2901321 GEO Accession GSM2901321 SRX3506687 GSM2901322 SRP127468 SRS2784230 GSM2901322 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901322 GSM2901322 GEO Accession GSM2901322 SRX3506688 GSM2901323 SRP127468 SRS2784231 GSM2901323 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901323 GSM2901323 GEO Accession GSM2901323 SRX3506689 GSM2901324 SRP127468 SRS2784239 GSM2901324 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901324 GSM2901324 GEO Accession GSM2901324 SRX3506690 GSM2901325 SRP127468 SRS2784245 GSM2901325 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901325 GSM2901325 GEO Accession GSM2901325 SRX3506691 GSM2901326 SRP127468 SRS2784232 GSM2901326 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using hot acid phenol method. For 4tU IP, 4tU residues in total RNA were biotinylated using HPDP-biotin; free HPDP-biotin removed and biotin-labeled RNA then purified on streptavidin beads, eluted from the column using beta-mercaptoethanol and RNA purified. Libraries were prepared using Lexogen QuantSeq REV kit (Lexogen GmbH, Vienna, Austria). Illumina HiSeq 2500 gds 302901326 GSM2901326 GEO Accession GSM2901326