SRX821994 GSM1571851 SRP051502 SRS801689 GSM1571851 ChIP-Seq GENOMIC ChIP After fixation, the cells were washed and sonicated using a Bioruptor (Diagenode) to generate chromatin extract. Chromatin extract was cleared by centrifugation and used in ChIP with affinity-purified anti-Drosophila CBP antibodies, pre-bound to a mix of Protein A and G Dynabeads. CBP bound DNA was purified, and sent to Uppsala Genome Center for SOLiD (TM) ChIP-Seq Library preparation (Rev date 18 March 2010), size selection (100-150 bp + adapters 90bp ≈250 bp), and SOLiD sequencing. Libraries were prepared for sequencing using standard SOLiD protocols AB SOLiD 4 System GEO Sample GSM1571851 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1571851 gds 301571851 GEO Accession GSM1571851 SRX821995 GSM1571852 SRP051502 SRS801690 GSM1571852 ChIP-Seq GENOMIC ChIP After fixation, the cells were washed and sonicated using a Bioruptor (Diagenode) to generate chromatin extract. Chromatin extract was cleared by centrifugation and used in ChIP with affinity-purified anti-Drosophila CBP antibodies, pre-bound to a mix of Protein A and G Dynabeads. CBP bound DNA was purified, and sent to Uppsala Genome Center for SOLiD (TM) ChIP-Seq Library preparation (Rev date 18 March 2010), size selection (100-150 bp + adapters 90bp ≈250 bp), and SOLiD sequencing. Libraries were prepared for sequencing using standard SOLiD protocols AB SOLiD 4 System GEO Sample GSM1571852 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1571852 gds 301571852 GEO Accession GSM1571852 SRX821996 GSM1571853 SRP051502 SRS801691 GSM1571853 ChIP-Seq GENOMIC ChIP After fixation, the cells were washed and sonicated using a Bioruptor (Diagenode) to generate chromatin extract. Chromatin extract was cleared by centrifugation and used in ChIP with affinity-purified anti-Drosophila CBP antibodies, pre-bound to a mix of Protein A and G Dynabeads. CBP bound DNA was purified, and sent to Uppsala Genome Center for SOLiD (TM) ChIP-Seq Library preparation (Rev date 18 March 2010), size selection (100-150 bp + adapters 90bp ≈250 bp), and SOLiD sequencing. Libraries were prepared for sequencing using standard SOLiD protocols AB SOLiD 4 System GEO Sample GSM1571853 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1571853 gds 301571853 GEO Accession GSM1571853 SRX821997 GSM1571854 SRP051502 SRS801692 GSM1571854 ChIP-Seq GENOMIC ChIP After fixation, the cells were washed and sonicated using a Bioruptor (Diagenode) to generate chromatin extract. Chromatin extract was cleared by centrifugation and used in ChIP with affinity-purified anti-Drosophila CBP antibodies, pre-bound to a mix of Protein A and G Dynabeads. CBP bound DNA was purified, and sent to Uppsala Genome Center for SOLiD (TM) ChIP-Seq Library preparation (Rev date 18 March 2010), size selection (100-150 bp + adapters 90bp ≈250 bp), and SOLiD sequencing. Libraries were prepared for sequencing using standard SOLiD protocols AB SOLiD 4 System GEO Sample GSM1571854 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1571854 gds 301571854 GEO Accession GSM1571854