SRX5188624 GSM3535194 SRP174669 SRS4194940 GSM3535194 ChIP-Seq GENOMIC ChIP ChIP experiment was performed using iDeal ChIP-seq kit for Transcription Factors (Diagenode SA, Belgium). Briefly, cells were fixed for 15 min at room temperature with 1% formaldehyde-containing medium. Nuclei were isolated and chromatin was sonicated in the mixture of shearing buffer and protease inhibitor cocktail to an average size of 220 bp. Sonicated chromatin was used for immunoprecipitation by incubation with anti-RUNX3 antibodies (ab11905, Abcam) (40 μg) overnight at 4ºC. One per cent of chromatin used for each ChIP reaction was kept as input DNA. Washed protein A-coated magnetic beads (120 μl) were added to each ChIP reaction and reactions were incubated 2 hr at 4ºC. The beads were then incubated in 400 μl elution buffer at 65ºC for 4 hr to elute immunoprecipitated materials. Libraries were prepared using DNA SMART ChIP-Seq Kit (Clontech Laboratories, USA), according to the manufacturer's protocol. Illumina HiSeq 2500 gds 303535194 GSM3535194 GEO Accession GSM3535194 SRX5188625 GSM3535195 SRP174669 SRS4194941 GSM3535195 ChIP-Seq GENOMIC ChIP ChIP experiment was performed using iDeal ChIP-seq kit for Transcription Factors (Diagenode SA, Belgium). Briefly, cells were fixed for 15 min at room temperature with 1% formaldehyde-containing medium. Nuclei were isolated and chromatin was sonicated in the mixture of shearing buffer and protease inhibitor cocktail to an average size of 220 bp. Sonicated chromatin was used for immunoprecipitation by incubation with anti-RUNX3 antibodies (ab11905, Abcam) (40 μg) overnight at 4ºC. One per cent of chromatin used for each ChIP reaction was kept as input DNA. Washed protein A-coated magnetic beads (120 μl) were added to each ChIP reaction and reactions were incubated 2 hr at 4ºC. The beads were then incubated in 400 μl elution buffer at 65ºC for 4 hr to elute immunoprecipitated materials. Libraries were prepared using DNA SMART ChIP-Seq Kit (Clontech Laboratories, USA), according to the manufacturer's protocol. Illumina HiSeq 2500 gds 303535195 GSM3535195 GEO Accession GSM3535195 SRX5188626 GSM3535196 SRP174669 SRS4194942 GSM3535196 ChIP-Seq GENOMIC ChIP ChIP experiment was performed using iDeal ChIP-seq kit for Transcription Factors (Diagenode SA, Belgium). Briefly, cells were fixed for 15 min at room temperature with 1% formaldehyde-containing medium. Nuclei were isolated and chromatin was sonicated in the mixture of shearing buffer and protease inhibitor cocktail to an average size of 220 bp. Sonicated chromatin was used for immunoprecipitation by incubation with anti-RUNX3 antibodies (ab11905, Abcam) (40 μg) overnight at 4ºC. One per cent of chromatin used for each ChIP reaction was kept as input DNA. Washed protein A-coated magnetic beads (120 μl) were added to each ChIP reaction and reactions were incubated 2 hr at 4ºC. The beads were then incubated in 400 μl elution buffer at 65ºC for 4 hr to elute immunoprecipitated materials. Libraries were prepared using DNA SMART ChIP-Seq Kit (Clontech Laboratories, USA), according to the manufacturer's protocol. Illumina HiSeq 2500 gds 303535196 GSM3535196 GEO Accession GSM3535196 SRX5188627 GSM3535197 SRP174669 SRS4194943 GSM3535197 ChIP-Seq GENOMIC ChIP ChIP experiment was performed using iDeal ChIP-seq kit for Transcription Factors (Diagenode SA, Belgium). Briefly, cells were fixed for 15 min at room temperature with 1% formaldehyde-containing medium. Nuclei were isolated and chromatin was sonicated in the mixture of shearing buffer and protease inhibitor cocktail to an average size of 220 bp. Sonicated chromatin was used for immunoprecipitation by incubation with anti-RUNX3 antibodies (ab11905, Abcam) (40 μg) overnight at 4ºC. One per cent of chromatin used for each ChIP reaction was kept as input DNA. Washed protein A-coated magnetic beads (120 μl) were added to each ChIP reaction and reactions were incubated 2 hr at 4ºC. The beads were then incubated in 400 μl elution buffer at 65ºC for 4 hr to elute immunoprecipitated materials. Libraries were prepared using DNA SMART ChIP-Seq Kit (Clontech Laboratories, USA), according to the manufacturer's protocol. Illumina HiSeq 2500 gds 303535197 GSM3535197 GEO Accession GSM3535197 SRX5188628 GSM3535198 SRP174669 SRS4194944 GSM3535198 ChIP-Seq GENOMIC ChIP ChIP experiment was performed using iDeal ChIP-seq kit for Transcription Factors (Diagenode SA, Belgium). Briefly, cells were fixed for 15 min at room temperature with 1% formaldehyde-containing medium. Nuclei were isolated and chromatin was sonicated in the mixture of shearing buffer and protease inhibitor cocktail to an average size of 220 bp. Sonicated chromatin was used for immunoprecipitation by incubation with anti-RUNX3 antibodies (ab11905, Abcam) (40 μg) overnight at 4ºC. One per cent of chromatin used for each ChIP reaction was kept as input DNA. Washed protein A-coated magnetic beads (120 μl) were added to each ChIP reaction and reactions were incubated 2 hr at 4ºC. The beads were then incubated in 400 μl elution buffer at 65ºC for 4 hr to elute immunoprecipitated materials. Libraries were prepared using DNA SMART ChIP-Seq Kit (Clontech Laboratories, USA), according to the manufacturer's protocol. Illumina HiSeq 2500 gds 303535198 GSM3535198 GEO Accession GSM3535198 SRX5188629 GSM3535199 SRP174669 SRS4194945 GSM3535199 ChIP-Seq GENOMIC ChIP ChIP experiment was performed using iDeal ChIP-seq kit for Transcription Factors (Diagenode SA, Belgium). Briefly, cells were fixed for 15 min at room temperature with 1% formaldehyde-containing medium. Nuclei were isolated and chromatin was sonicated in the mixture of shearing buffer and protease inhibitor cocktail to an average size of 220 bp. Sonicated chromatin was used for immunoprecipitation by incubation with anti-RUNX3 antibodies (ab11905, Abcam) (40 μg) overnight at 4ºC. One per cent of chromatin used for each ChIP reaction was kept as input DNA. Washed protein A-coated magnetic beads (120 μl) were added to each ChIP reaction and reactions were incubated 2 hr at 4ºC. The beads were then incubated in 400 μl elution buffer at 65ºC for 4 hr to elute immunoprecipitated materials. Libraries were prepared using DNA SMART ChIP-Seq Kit (Clontech Laboratories, USA), according to the manufacturer's protocol. Illumina HiSeq 2500 gds 303535199 GSM3535199 GEO Accession GSM3535199 SRX5188630 GSM3535200 SRP174669 SRS4194946 GSM3535200 ChIP-Seq GENOMIC ChIP ChIP experiment was performed using iDeal ChIP-seq kit for Transcription Factors (Diagenode SA, Belgium). Briefly, cells were fixed for 15 min at room temperature with 1% formaldehyde-containing medium. Nuclei were isolated and chromatin was sonicated in the mixture of shearing buffer and protease inhibitor cocktail to an average size of 220 bp. Sonicated chromatin was used for immunoprecipitation by incubation with anti-RUNX3 antibodies (ab11905, Abcam) (40 μg) overnight at 4ºC. One per cent of chromatin used for each ChIP reaction was kept as input DNA. Washed protein A-coated magnetic beads (120 μl) were added to each ChIP reaction and reactions were incubated 2 hr at 4ºC. The beads were then incubated in 400 μl elution buffer at 65ºC for 4 hr to elute immunoprecipitated materials. Libraries were prepared using DNA SMART ChIP-Seq Kit (Clontech Laboratories, USA), according to the manufacturer's protocol. Illumina HiSeq 2500 gds 303535200 GSM3535200 GEO Accession GSM3535200 SRX5188631 GSM3535201 SRP174669 SRS4194947 GSM3535201 ChIP-Seq GENOMIC ChIP ChIP experiment was performed using iDeal ChIP-seq kit for Transcription Factors (Diagenode SA, Belgium). Briefly, cells were fixed for 15 min at room temperature with 1% formaldehyde-containing medium. Nuclei were isolated and chromatin was sonicated in the mixture of shearing buffer and protease inhibitor cocktail to an average size of 220 bp. Sonicated chromatin was used for immunoprecipitation by incubation with anti-RUNX3 antibodies (ab11905, Abcam) (40 μg) overnight at 4ºC. One per cent of chromatin used for each ChIP reaction was kept as input DNA. Washed protein A-coated magnetic beads (120 μl) were added to each ChIP reaction and reactions were incubated 2 hr at 4ºC. The beads were then incubated in 400 μl elution buffer at 65ºC for 4 hr to elute immunoprecipitated materials. Libraries were prepared using DNA SMART ChIP-Seq Kit (Clontech Laboratories, USA), according to the manufacturer's protocol. Illumina HiSeq 2500 gds 303535201 GSM3535201 GEO Accession GSM3535201 SRX5188632 GSM3535202 SRP174669 SRS4194948 GSM3535202 ChIP-Seq GENOMIC ChIP ChIP experiment was performed using iDeal ChIP-seq kit for Transcription Factors (Diagenode SA, Belgium). Briefly, cells were fixed for 15 min at room temperature with 1% formaldehyde-containing medium. Nuclei were isolated and chromatin was sonicated in the mixture of shearing buffer and protease inhibitor cocktail to an average size of 220 bp. Sonicated chromatin was used for immunoprecipitation by incubation with anti-RUNX3 antibodies (ab11905, Abcam) (40 μg) overnight at 4ºC. One per cent of chromatin used for each ChIP reaction was kept as input DNA. Washed protein A-coated magnetic beads (120 μl) were added to each ChIP reaction and reactions were incubated 2 hr at 4ºC. The beads were then incubated in 400 μl elution buffer at 65ºC for 4 hr to elute immunoprecipitated materials. Libraries were prepared using DNA SMART ChIP-Seq Kit (Clontech Laboratories, USA), according to the manufacturer's protocol. Illumina HiSeq 2500 gds 303535202 GSM3535202 GEO Accession GSM3535202 SRX5188633 GSM3535203 SRP174669 SRS4194949 GSM3535203 ChIP-Seq GENOMIC ChIP ChIP experiment was performed using iDeal ChIP-seq kit for Transcription Factors (Diagenode SA, Belgium). Briefly, cells were fixed for 15 min at room temperature with 1% formaldehyde-containing medium. Nuclei were isolated and chromatin was sonicated in the mixture of shearing buffer and protease inhibitor cocktail to an average size of 220 bp. Sonicated chromatin was used for immunoprecipitation by incubation with anti-RUNX3 antibodies (ab11905, Abcam) (40 μg) overnight at 4ºC. One per cent of chromatin used for each ChIP reaction was kept as input DNA. Washed protein A-coated magnetic beads (120 μl) were added to each ChIP reaction and reactions were incubated 2 hr at 4ºC. The beads were then incubated in 400 μl elution buffer at 65ºC for 4 hr to elute immunoprecipitated materials. Libraries were prepared using DNA SMART ChIP-Seq Kit (Clontech Laboratories, USA), according to the manufacturer's protocol. Illumina HiSeq 2500 gds 303535203 GSM3535203 GEO Accession GSM3535203 SRX5188634 GSM3535204 SRP174669 SRS4194950 GSM3535204 ChIP-Seq GENOMIC ChIP ChIP experiment was performed using iDeal ChIP-seq kit for Transcription Factors (Diagenode SA, Belgium). Briefly, cells were fixed for 15 min at room temperature with 1% formaldehyde-containing medium. Nuclei were isolated and chromatin was sonicated in the mixture of shearing buffer and protease inhibitor cocktail to an average size of 220 bp. Sonicated chromatin was used for immunoprecipitation by incubation with anti-RUNX3 antibodies (ab11905, Abcam) (40 μg) overnight at 4ºC. One per cent of chromatin used for each ChIP reaction was kept as input DNA. Washed protein A-coated magnetic beads (120 μl) were added to each ChIP reaction and reactions were incubated 2 hr at 4ºC. The beads were then incubated in 400 μl elution buffer at 65ºC for 4 hr to elute immunoprecipitated materials. Libraries were prepared using DNA SMART ChIP-Seq Kit (Clontech Laboratories, USA), according to the manufacturer's protocol. Illumina HiSeq 2500 gds 303535204 GSM3535204 GEO Accession GSM3535204 SRX5188635 GSM3535205 SRP174669 SRS4194951 GSM3535205 ChIP-Seq GENOMIC ChIP ChIP experiment was performed using iDeal ChIP-seq kit for Transcription Factors (Diagenode SA, Belgium). Briefly, cells were fixed for 15 min at room temperature with 1% formaldehyde-containing medium. Nuclei were isolated and chromatin was sonicated in the mixture of shearing buffer and protease inhibitor cocktail to an average size of 220 bp. Sonicated chromatin was used for immunoprecipitation by incubation with anti-RUNX3 antibodies (ab11905, Abcam) (40 μg) overnight at 4ºC. One per cent of chromatin used for each ChIP reaction was kept as input DNA. Washed protein A-coated magnetic beads (120 μl) were added to each ChIP reaction and reactions were incubated 2 hr at 4ºC. The beads were then incubated in 400 μl elution buffer at 65ºC for 4 hr to elute immunoprecipitated materials. Libraries were prepared using DNA SMART ChIP-Seq Kit (Clontech Laboratories, USA), according to the manufacturer's protocol. Illumina HiSeq 2500 gds 303535205 GSM3535205 GEO Accession GSM3535205