SRX3511102 GSM2902640 SRP127542 SRS2791635 GSM2902640 ChIP-Seq GENOMIC ChIP The chromatin was decross-linked at 65 oC over night in TE buffer with 1% SDS, 500 mM NaCl, 20 ug of Proteinase K. DNA was extracted and purified with Qiagen MinElute kit. After reverse crosslinking, ChIP and input DNA fragments were used for library construction with NEBNext Ultra Ligation Module (E7445, NEB) Illumina HiSeq 4000 gds 302902640 GSM2902640 GEO Accession GSM2902640 SRX3511103 GSM2902641 SRP127542 SRS2791637 GSM2902641 ChIP-Seq GENOMIC ChIP The chromatin was decross-linked at 65 oC over night in TE buffer with 1% SDS, 500 mM NaCl, 20 ug of Proteinase K. DNA was extracted and purified with Qiagen MinElute kit. After reverse crosslinking, ChIP and input DNA fragments were used for library construction with NEBNext Ultra Ligation Module (E7445, NEB) Illumina HiSeq 4000 gds 302902641 GSM2902641 GEO Accession GSM2902641 SRX3511104 GSM2902642 SRP127542 SRS2791636 GSM2902642 ChIP-Seq GENOMIC ChIP The chromatin was decross-linked at 65 oC over night in TE buffer with 1% SDS, 500 mM NaCl, 20 ug of Proteinase K. DNA was extracted and purified with Qiagen MinElute kit. After reverse crosslinking, ChIP and input DNA fragments were used for library construction with NEBNext Ultra Ligation Module (E7445, NEB) Illumina HiSeq 4000 gds 302902642 GSM2902642 GEO Accession GSM2902642 SRX3511105 GSM2902643 SRP127542 SRS2791638 GSM2902643 ChIP-Seq GENOMIC ChIP The chromatin was decross-linked at 65 oC over night in TE buffer with 1% SDS, 500 mM NaCl, 20 ug of Proteinase K. DNA was extracted and purified with Qiagen MinElute kit. After reverse crosslinking, ChIP and input DNA fragments were used for library construction with NEBNext Ultra Ligation Module (E7445, NEB) Illumina HiSeq 4000 gds 302902643 GSM2902643 GEO Accession GSM2902643