SRX23755200 GSM8112500_r1 SRP491875 PRJNA1080559 SRS20581390 GSM8112500 GSM8112500 ChIP-Seq GENOMIC ChIP The sample was fixed in 1% formaldehyde for Cross-Linking of DNA and Protein,after which 0.125M glycine was added and the mixture was sat to terminate the crosslinking reaction. Extract chromatin from samples by adding Lysis Buffer.Then, samples was sonicated to fragment chromatin DNA. The 10% lysis sonicated chromatin was stored and named “input”, and 90% was used in immunoprecipitation reactions with antibody and named “IP”. The sequencing libraries of input and IP were generated by NEBNext® UltraTM DNA Library Prep Kit for Illumina.An A-base was added to the fragmented DNA ends and adapter was ligated.After purification with beads, products are amplified with PCR for 8-10 cycles. The library products corresponding to 100-500 bps were enriched, quantified and finally sequenced on Novaseq 6000 sequencer (Illumina) with PE150 model. Illumina NovaSeq 6000 SRX23755201 GSM8112501_r1 SRP491875 PRJNA1080559 SRS20581275 GSM8112501 GSM8112501 ChIP-Seq GENOMIC ChIP The sample was fixed in 1% formaldehyde for Cross-Linking of DNA and Protein,after which 0.125M glycine was added and the mixture was sat to terminate the crosslinking reaction. Extract chromatin from samples by adding Lysis Buffer.Then, samples was sonicated to fragment chromatin DNA. The 10% lysis sonicated chromatin was stored and named “input”, and 90% was used in immunoprecipitation reactions with antibody and named “IP”. The sequencing libraries of input and IP were generated by NEBNext® UltraTM DNA Library Prep Kit for Illumina.An A-base was added to the fragmented DNA ends and adapter was ligated.After purification with beads, products are amplified with PCR for 8-10 cycles. The library products corresponding to 100-500 bps were enriched, quantified and finally sequenced on Novaseq 6000 sequencer (Illumina) with PE150 model. Illumina NovaSeq 6000 SRX23755202 GSM8112502_r1 SRP491875 PRJNA1080559 SRS20580822 GSM8112502 GSM8112502 ChIP-Seq GENOMIC ChIP The sample was fixed in 1% formaldehyde for Cross-Linking of DNA and Protein,after which 0.125M glycine was added and the mixture was sat to terminate the crosslinking reaction. Extract chromatin from samples by adding Lysis Buffer.Then, samples was sonicated to fragment chromatin DNA. The 10% lysis sonicated chromatin was stored and named “input”, and 90% was used in immunoprecipitation reactions with antibody and named “IP”. The sequencing libraries of input and IP were generated by NEBNext® UltraTM DNA Library Prep Kit for Illumina.An A-base was added to the fragmented DNA ends and adapter was ligated.After purification with beads, products are amplified with PCR for 8-10 cycles. The library products corresponding to 100-500 bps were enriched, quantified and finally sequenced on Novaseq 6000 sequencer (Illumina) with PE150 model. Illumina NovaSeq 6000 SRX23755203 GSM8112503_r1 SRP491875 PRJNA1080559 SRS20581278 GSM8112503 GSM8112503 ChIP-Seq GENOMIC ChIP The sample was fixed in 1% formaldehyde for Cross-Linking of DNA and Protein,after which 0.125M glycine was added and the mixture was sat to terminate the crosslinking reaction. Extract chromatin from samples by adding Lysis Buffer.Then, samples was sonicated to fragment chromatin DNA. The 10% lysis sonicated chromatin was stored and named “input”, and 90% was used in immunoprecipitation reactions with antibody and named “IP”. The sequencing libraries of input and IP were generated by NEBNext® UltraTM DNA Library Prep Kit for Illumina.An A-base was added to the fragmented DNA ends and adapter was ligated.After purification with beads, products are amplified with PCR for 8-10 cycles. The library products corresponding to 100-500 bps were enriched, quantified and finally sequenced on Novaseq 6000 sequencer (Illumina) with PE150 model. Illumina NovaSeq 6000