SRX7794503 GSM4337012 SRP118897 PRJNA412202 SRS6209897 GSM4337012 ChIP-Seq GENOMIC ChIP ChIP assays were performed using a ChIP assay kit (Upstate Biotechnology, Cat No: 17-295) per the manufacturer's instructions. Briefly, cells were double crosslinked with 10 mM DTBP for 10 min at room temperature, followed by incubation in 1% formaldehyde for 15 min in a 37 °C water bath. Nuclei were extracted and sonication was perfromed to generate 200–500 bp genomic DNA fragments. Chromatin complexes were immunoprecipitated with the related antibodies and Dynabeads Protein A/G. The precipitated DNA was purified using DNA clean and concentrator (Zymo Research). Libraries were prepared using KAPA Hyper Prep Kit (Kapa Biosystems, Cat No: KK8502) Illumina HiSeq 3000 gds 304337012 GSM4337012 GEO Accession GSM4337012 SRX7794504 GSM4337013 SRP118897 PRJNA412202 SRS6209898 GSM4337013 ChIP-Seq GENOMIC ChIP ChIP assays were performed using a ChIP assay kit (Upstate Biotechnology, Cat No: 17-295) per the manufacturer's instructions. Briefly, cells were double crosslinked with 10 mM DTBP for 10 min at room temperature, followed by incubation in 1% formaldehyde for 15 min in a 37 °C water bath. Nuclei were extracted and sonication was perfromed to generate 200–500 bp genomic DNA fragments. Chromatin complexes were immunoprecipitated with the related antibodies and Dynabeads Protein A/G. The precipitated DNA was purified using DNA clean and concentrator (Zymo Research). Libraries were prepared using KAPA Hyper Prep Kit (Kapa Biosystems, Cat No: KK8502) Illumina HiSeq 3000 gds 304337013 GSM4337013 GEO Accession GSM4337013 SRX8061036 GSM4454172 SRP118897 PRJNA412202 SRS6429687 GSM4454172 ChIP-Seq GENOMIC ChIP ChIP assays were performed using a ChIP assay kit (Upstate Biotechnology, Cat No: 17-295) per the manufacturer's instructions. Briefly, cells were double crosslinked with 10 mM DTBP for 10 min at room temperature, followed by incubation in 1% formaldehyde for 15 min in a 37 °C water bath. Nuclei were extracted and sonication was perfromed to generate 200–500 bp genomic DNA fragments. Chromatin complexes were immunoprecipitated with the related antibodies and Dynabeads Protein A/G. The precipitated DNA was purified using DNA clean and concentrator (Zymo Research). Libraries were prepared using KAPA Hyper Prep Kit (Kapa Biosystems, Cat No: KK8502) NextSeq 500 gds 304454172 GSM4454172 GEO Accession GSM4454172 SRX8061037 GSM4454173 SRP118897 PRJNA412202 SRS6429688 GSM4454173 ChIP-Seq GENOMIC ChIP ChIP assays were performed using a ChIP assay kit (Upstate Biotechnology, Cat No: 17-295) per the manufacturer's instructions. Briefly, cells were double crosslinked with 10 mM DTBP for 10 min at room temperature, followed by incubation in 1% formaldehyde for 15 min in a 37 °C water bath. Nuclei were extracted and sonication was perfromed to generate 200–500 bp genomic DNA fragments. Chromatin complexes were immunoprecipitated with the related antibodies and Dynabeads Protein A/G. The precipitated DNA was purified using DNA clean and concentrator (Zymo Research). Libraries were prepared using KAPA Hyper Prep Kit (Kapa Biosystems, Cat No: KK8502) NextSeq 500 gds 304454173 GSM4454173 GEO Accession GSM4454173 SRX8061038 GSM4454174 SRP118897 PRJNA412202 SRS6429689 GSM4454174 ChIP-Seq GENOMIC ChIP ChIP assays were performed using a ChIP assay kit (Upstate Biotechnology, Cat No: 17-295) per the manufacturer's instructions. Briefly, cells were double crosslinked with 10 mM DTBP for 10 min at room temperature, followed by incubation in 1% formaldehyde for 15 min in a 37 °C water bath. Nuclei were extracted and sonication was perfromed to generate 200–500 bp genomic DNA fragments. Chromatin complexes were immunoprecipitated with the related antibodies and Dynabeads Protein A/G. The precipitated DNA was purified using DNA clean and concentrator (Zymo Research). Libraries were prepared using KAPA Hyper Prep Kit (Kapa Biosystems, Cat No: KK8502) Illumina HiSeq 3000 gds 304454174 GSM4454174 GEO Accession GSM4454174 SRX8061039 GSM4454175 SRP118897 PRJNA412202 SRS6429690 GSM4454175 ChIP-Seq GENOMIC ChIP ChIP assays were performed using a ChIP assay kit (Upstate Biotechnology, Cat No: 17-295) per the manufacturer's instructions. Briefly, cells were double crosslinked with 10 mM DTBP for 10 min at room temperature, followed by incubation in 1% formaldehyde for 15 min in a 37 °C water bath. Nuclei were extracted and sonication was perfromed to generate 200–500 bp genomic DNA fragments. Chromatin complexes were immunoprecipitated with the related antibodies and Dynabeads Protein A/G. The precipitated DNA was purified using DNA clean and concentrator (Zymo Research). Libraries were prepared using KAPA Hyper Prep Kit (Kapa Biosystems, Cat No: KK8502) Illumina HiSeq 3000 gds 304454175 GSM4454175 GEO Accession GSM4454175 SRX8061040 GSM4454176 SRP118897 PRJNA412202 SRS6429691 GSM4454176 ChIP-Seq GENOMIC ChIP ChIP assays were performed using a ChIP assay kit (Upstate Biotechnology, Cat No: 17-295) per the manufacturer's instructions. Briefly, cells were double crosslinked with 10 mM DTBP for 10 min at room temperature, followed by incubation in 1% formaldehyde for 15 min in a 37 °C water bath. Nuclei were extracted and sonication was perfromed to generate 200–500 bp genomic DNA fragments. Chromatin complexes were immunoprecipitated with the related antibodies and Dynabeads Protein A/G. The precipitated DNA was purified using DNA clean and concentrator (Zymo Research). Libraries were prepared using KAPA Hyper Prep Kit (Kapa Biosystems, Cat No: KK8502) Illumina HiSeq 3000 gds 304454176 GSM4454176 GEO Accession GSM4454176 SRX8061041 GSM4454177 SRP118897 PRJNA412202 SRS6429692 GSM4454177 ChIP-Seq GENOMIC ChIP ChIP assays were performed using a ChIP assay kit (Upstate Biotechnology, Cat No: 17-295) per the manufacturer's instructions. Briefly, cells were double crosslinked with 10 mM DTBP for 10 min at room temperature, followed by incubation in 1% formaldehyde for 15 min in a 37 °C water bath. Nuclei were extracted and sonication was perfromed to generate 200–500 bp genomic DNA fragments. Chromatin complexes were immunoprecipitated with the related antibodies and Dynabeads Protein A/G. The precipitated DNA was purified using DNA clean and concentrator (Zymo Research). Libraries were prepared using KAPA Hyper Prep Kit (Kapa Biosystems, Cat No: KK8502) Illumina HiSeq 3000 gds 304454177 GSM4454177 GEO Accession GSM4454177