SRX11230145 GSM5400956 SRP325637 SRS9279508 GSM5400956 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400956 GSM5400956 GEO Accession GSM5400956 SRX11230146 GSM5400957 SRP325637 SRS9279510 GSM5400957 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400957 GSM5400957 GEO Accession GSM5400957 SRX11230147 GSM5400958 SRP325637 SRS9279512 GSM5400958 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400958 GSM5400958 GEO Accession GSM5400958 SRX11230148 GSM5400959 SRP325637 SRS9279511 GSM5400959 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400959 GSM5400959 GEO Accession GSM5400959 SRX11230149 GSM5400960 SRP325637 SRS9279514 GSM5400960 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400960 GSM5400960 GEO Accession GSM5400960 SRX11230150 GSM5400961 SRP325637 SRS9279513 GSM5400961 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400961 GSM5400961 GEO Accession GSM5400961 SRX11230151 GSM5400962 SRP325637 SRS9279515 GSM5400962 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400962 GSM5400962 GEO Accession GSM5400962 SRX11230152 GSM5400963 SRP325637 SRS9279517 GSM5400963 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400963 GSM5400963 GEO Accession GSM5400963 SRX11230153 GSM5400964 SRP325637 SRS9279516 GSM5400964 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400964 GSM5400964 GEO Accession GSM5400964 SRX11230154 GSM5400965 SRP325637 SRS9279518 GSM5400965 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400965 GSM5400965 GEO Accession GSM5400965 SRX11230155 GSM5400966 SRP325637 SRS9279519 GSM5400966 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400966 GSM5400966 GEO Accession GSM5400966 SRX11230156 GSM5400967 SRP325637 SRS9279521 GSM5400967 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400967 GSM5400967 GEO Accession GSM5400967 SRX11230157 GSM5400968 SRP325637 SRS9279520 GSM5400968 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400968 GSM5400968 GEO Accession GSM5400968 SRX11230158 GSM5400969 SRP325637 SRS9279522 GSM5400969 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400969 GSM5400969 GEO Accession GSM5400969 SRX11230159 GSM5400970 SRP325637 SRS9279523 GSM5400970 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400970 GSM5400970 GEO Accession GSM5400970 SRX11230160 GSM5400971 SRP325637 SRS9279524 GSM5400971 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400971 GSM5400971 GEO Accession GSM5400971 SRX11230161 GSM5400972 SRP325637 SRS9279525 GSM5400972 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400972 GSM5400972 GEO Accession GSM5400972 SRX11230162 GSM5400973 SRP325637 SRS9279526 GSM5400973 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400973 GSM5400973 GEO Accession GSM5400973 SRX11230163 GSM5400974 SRP325637 SRS9279528 GSM5400974 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400974 GSM5400974 GEO Accession GSM5400974 SRX11230164 GSM5400975 SRP325637 SRS9279527 GSM5400975 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400975 GSM5400975 GEO Accession GSM5400975 SRX11230166 GSM5400977 SRP325637 SRS9279531 GSM5400977 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400977 GSM5400977 GEO Accession GSM5400977 SRX11230167 GSM5400978 SRP325637 SRS9279530 GSM5400978 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400978 GSM5400978 GEO Accession GSM5400978 SRX11230168 GSM5400979 SRP325637 SRS9279532 GSM5400979 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400979 GSM5400979 GEO Accession GSM5400979 SRX11230169 GSM5400980 SRP325637 SRS9279534 GSM5400980 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400980 GSM5400980 GEO Accession GSM5400980 SRX11230170 GSM5400981 SRP325637 SRS9279533 GSM5400981 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400981 GSM5400981 GEO Accession GSM5400981 SRX11230171 GSM5400982 SRP325637 SRS9279535 GSM5400982 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400982 GSM5400982 GEO Accession GSM5400982 SRX11230172 GSM5400983 SRP325637 SRS9279536 GSM5400983 RNA-Seq TRANSCRIPTOMIC cDNA The cells including untreated controls were washed and total RNA isolated using RNeasy mini kit (Qiagen©, Germany) following the manufacturers' protocol. RNA integrity was verified using 2100 Bioanalyzer (Agilent Technologies Inc., CA, USA) and adjusted to an acceptable concentration. Libraries were generated from the RNA using Illumina stranded mRNA kit (Illumina Inc., CA, USA) and sequenced on an Illumina NextSeq500 system (Illumina Inc., CA, USA) using 75 bp single reads. Obtained reads were aligned against the reference human genome (UCSC hg19) using STARalign v2.5.0. NextSeq 500 gds 305400983 GSM5400983 GEO Accession GSM5400983