SRX2334041 GSM2385535 SRP058847 SRS1787933 GSM2385535 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385535 GEO Accession GSM2385535 SRX2334042 GSM2385536 SRP058847 SRS1787934 GSM2385536 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385536 GEO Accession GSM2385536 SRX2334043 GSM2385537 SRP058847 SRS1787935 GSM2385537 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385537 GEO Accession GSM2385537 SRX2334044 GSM2385538 SRP058847 SRS1787936 GSM2385538 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385538 GEO Accession GSM2385538 SRX2334045 GSM2385539 SRP058847 SRS1787937 GSM2385539 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385539 GEO Accession GSM2385539 SRX2334046 GSM2385540 SRP058847 SRS1787938 GSM2385540 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385540 GEO Accession GSM2385540 SRX2334047 GSM2385541 SRP058847 SRS1787939 GSM2385541 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385541 GEO Accession GSM2385541 SRX2334048 GSM2385542 SRP058847 SRS1787940 GSM2385542 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385542 GEO Accession GSM2385542 SRX2334049 GSM2385543 SRP058847 SRS1787941 GSM2385543 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385543 GEO Accession GSM2385543 SRX2334050 GSM2385544 SRP058847 SRS1787942 GSM2385544 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385544 GEO Accession GSM2385544 SRX2334051 GSM2385545 SRP058847 SRS1787943 GSM2385545 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385545 GEO Accession GSM2385545 SRX2334052 GSM2385546 SRP058847 SRS1787944 GSM2385546 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385546 GEO Accession GSM2385546 SRX2334053 GSM2385547 SRP058847 SRS1787945 GSM2385547 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385547 GEO Accession GSM2385547 SRX2334054 GSM2385548 SRP058847 SRS1787946 GSM2385548 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from EpH4 and EpRas cells using the RNeasy Mini Kit (Qiagen) and Dnase-treated. siRNA-untransfected samples and siRNA-transfected samples were processed independently. mRNA was purified using Dynabeads mRNA DIRECT Purification Kit. Libraries were made using Ion Total RNA-Seq Kit v2 and directionally sequenced with the Ion Proton using Ion PI chip v2, Ion Proton IC200 kit, as described (Isogaya et al., Cell Res, 2014; Mizutani et al., 2016, Oncogene). Ion Torrent Proton gds 302385548 GEO Accession GSM2385548