SRX3511927 GSM2902689 SRP127546 SRS2792236 GSM2902689 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibodies againts the specific proteins of interest in each case. DNA libraries were prepared using the Illumina TruSeq RNA sample preparation Kit v2 starting from the end repair step of the protocol. Up to 100 ng ChIP DNA was used as starting material. After end repair and A-tailing, indexing adapters were ligated. The products were then purified and amplified for 18 PCR cycles to create the final libraries. Illumina HiSeq 2500 gds 302902689 GSM2902689 GEO Accession GSM2902689 SRX3511928 GSM2902690 SRP127546 SRS2792235 GSM2902690 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibodies againts the specific proteins of interest in each case. DNA libraries were prepared using the Illumina TruSeq RNA sample preparation Kit v2 starting from the end repair step of the protocol. Up to 100 ng ChIP DNA was used as starting material. After end repair and A-tailing, indexing adapters were ligated. The products were then purified and amplified for 18 PCR cycles to create the final libraries. Illumina HiSeq 2500 gds 302902690 GSM2902690 GEO Accession GSM2902690 SRX3511929 GSM2902691 SRP127546 SRS2792237 GSM2902691 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibodies againts the specific proteins of interest in each case. DNA libraries were prepared using the Illumina TruSeq RNA sample preparation Kit v2 starting from the end repair step of the protocol. Up to 100 ng ChIP DNA was used as starting material. After end repair and A-tailing, indexing adapters were ligated. The products were then purified and amplified for 18 PCR cycles to create the final libraries. Illumina HiSeq 2500 gds 302902691 GSM2902691 GEO Accession GSM2902691 SRX3511930 GSM2902692 SRP127546 SRS2792239 GSM2902692 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibodies againts the specific proteins of interest in each case. DNA libraries were prepared using the Illumina TruSeq RNA sample preparation Kit v2 starting from the end repair step of the protocol. Up to 100 ng ChIP DNA was used as starting material. After end repair and A-tailing, indexing adapters were ligated. The products were then purified and amplified for 18 PCR cycles to create the final libraries. Illumina HiSeq 2500 gds 302902692 GSM2902692 GEO Accession GSM2902692 SRX3511931 GSM2902693 SRP127546 SRS2792240 GSM2902693 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibodies againts the specific proteins of interest in each case. DNA libraries were prepared using the Illumina TruSeq RNA sample preparation Kit v2 starting from the end repair step of the protocol. Up to 100 ng ChIP DNA was used as starting material. After end repair and A-tailing, indexing adapters were ligated. The products were then purified and amplified for 18 PCR cycles to create the final libraries. Illumina HiSeq 2500 gds 302902693 GSM2902693 GEO Accession GSM2902693 SRX3511932 GSM2902694 SRP127546 SRS2792238 GSM2902694 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibodies againts the specific proteins of interest in each case. DNA libraries were prepared using the Illumina TruSeq RNA sample preparation Kit v2 starting from the end repair step of the protocol. Up to 100 ng ChIP DNA was used as starting material. After end repair and A-tailing, indexing adapters were ligated. The products were then purified and amplified for 18 PCR cycles to create the final libraries. Illumina HiSeq 2500 gds 302902694 GSM2902694 GEO Accession GSM2902694 SRX3511933 GSM2902695 SRP127546 SRS2792241 GSM2902695 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibodies againts the specific proteins of interest in each case. DNA libraries were prepared using the Illumina TruSeq RNA sample preparation Kit v2 starting from the end repair step of the protocol. Up to 100 ng ChIP DNA was used as starting material. After end repair and A-tailing, indexing adapters were ligated. The products were then purified and amplified for 18 PCR cycles to create the final libraries. Illumina HiSeq 2500 gds 302902695 GSM2902695 GEO Accession GSM2902695 SRX3511934 GSM2902696 SRP127546 SRS2792244 GSM2902696 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibodies againts the specific proteins of interest in each case. DNA libraries were prepared using the Illumina TruSeq RNA sample preparation Kit v2 starting from the end repair step of the protocol. Up to 100 ng ChIP DNA was used as starting material. After end repair and A-tailing, indexing adapters were ligated. The products were then purified and amplified for 18 PCR cycles to create the final libraries. Illumina HiSeq 2500 gds 302902696 GSM2902696 GEO Accession GSM2902696 SRX3511935 GSM2902697 SRP127546 SRS2792242 GSM2902697 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibodies againts the specific proteins of interest in each case. DNA libraries were prepared using the Illumina TruSeq RNA sample preparation Kit v2 starting from the end repair step of the protocol. Up to 100 ng ChIP DNA was used as starting material. After end repair and A-tailing, indexing adapters were ligated. The products were then purified and amplified for 18 PCR cycles to create the final libraries. Illumina HiSeq 2500 gds 302902697 GSM2902697 GEO Accession GSM2902697 SRX3511936 GSM2902698 SRP127546 SRS2792243 GSM2902698 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibodies againts the specific proteins of interest in each case. DNA libraries were prepared using the Illumina TruSeq RNA sample preparation Kit v2 starting from the end repair step of the protocol. Up to 100 ng ChIP DNA was used as starting material. After end repair and A-tailing, indexing adapters were ligated. The products were then purified and amplified for 18 PCR cycles to create the final libraries. Illumina HiSeq 2500 gds 302902698 GSM2902698 GEO Accession GSM2902698 SRX3511937 GSM2902699 SRP127546 SRS2792246 GSM2902699 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibodies againts the specific proteins of interest in each case. DNA libraries were prepared using the Illumina TruSeq RNA sample preparation Kit v2 starting from the end repair step of the protocol. Up to 100 ng ChIP DNA was used as starting material. After end repair and A-tailing, indexing adapters were ligated. The products were then purified and amplified for 18 PCR cycles to create the final libraries. Illumina HiSeq 2500 gds 302902699 GSM2902699 GEO Accession GSM2902699 SRX3511938 GSM2902700 SRP127546 SRS2792245 GSM2902700 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibodies againts the specific proteins of interest in each case. DNA libraries were prepared using the Illumina TruSeq RNA sample preparation Kit v2 starting from the end repair step of the protocol. Up to 100 ng ChIP DNA was used as starting material. After end repair and A-tailing, indexing adapters were ligated. The products were then purified and amplified for 18 PCR cycles to create the final libraries. Illumina HiSeq 2500 gds 302902700 GSM2902700 GEO Accession GSM2902700 SRX3511939 GSM2902701 SRP127546 SRS2792248 GSM2902701 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibodies againts the specific proteins of interest in each case. DNA libraries were prepared using the Illumina TruSeq RNA sample preparation Kit v2 starting from the end repair step of the protocol. Up to 100 ng ChIP DNA was used as starting material. After end repair and A-tailing, indexing adapters were ligated. The products were then purified and amplified for 18 PCR cycles to create the final libraries. Illumina HiSeq 2500 gds 302902701 GSM2902701 GEO Accession GSM2902701