SRX1838916 GSM2197808 SRP076476 SRS1498123 GSM2197808 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197808 GEO Accession GSM2197808 SRX1838917 GSM2197809 SRP076476 SRS1498124 GSM2197809 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197809 GEO Accession GSM2197809 SRX1838918 GSM2197810 SRP076476 SRS1498128 GSM2197810 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197810 GEO Accession GSM2197810 SRX1838919 GSM2197811 SRP076476 SRS1498125 GSM2197811 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197811 GEO Accession GSM2197811 SRX1838920 GSM2197812 SRP076476 SRS1498126 GSM2197812 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197812 GEO Accession GSM2197812 SRX1838921 GSM2197813 SRP076476 SRS1498127 GSM2197813 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197813 GEO Accession GSM2197813 SRX1838922 GSM2197814 SRP076476 SRS1498129 GSM2197814 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197814 GEO Accession GSM2197814 SRX1838923 GSM2197815 SRP076476 SRS1498130 GSM2197815 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197815 GEO Accession GSM2197815 SRX1838924 GSM2197816 SRP076476 SRS1498131 GSM2197816 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197816 GEO Accession GSM2197816 SRX1838925 GSM2197817 SRP076476 SRS1498132 GSM2197817 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197817 GEO Accession GSM2197817 SRX1838926 GSM2197818 SRP076476 SRS1498133 GSM2197818 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197818 GEO Accession GSM2197818 SRX1838927 GSM2197819 SRP076476 SRS1498134 GSM2197819 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197819 GEO Accession GSM2197819 SRX1838928 GSM2197820 SRP076476 SRS1498135 GSM2197820 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197820 GEO Accession GSM2197820 SRX1838929 GSM2197821 SRP076476 SRS1498136 GSM2197821 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197821 GEO Accession GSM2197821 SRX1838930 GSM2197822 SRP076476 SRS1498138 GSM2197822 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197822 GEO Accession GSM2197822 SRX1838931 GSM2197823 SRP076476 SRS1498137 GSM2197823 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197823 GEO Accession GSM2197823 SRX1838932 GSM2197824 SRP076476 SRS1498139 GSM2197824 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197824 GEO Accession GSM2197824 SRX1838933 GSM2197825 SRP076476 SRS1498140 GSM2197825 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197825 GEO Accession GSM2197825 SRX1838934 GSM2197826 SRP076476 SRS1498141 GSM2197826 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197826 GEO Accession GSM2197826 SRX1838935 GSM2197827 SRP076476 SRS1498142 GSM2197827 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197827 GEO Accession GSM2197827 SRX1838936 GSM2197828 SRP076476 SRS1498143 GSM2197828 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197828 GEO Accession GSM2197828 SRX1838937 GSM2197829 SRP076476 SRS1498144 GSM2197829 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197829 GEO Accession GSM2197829 SRX1838938 GSM2197830 SRP076476 SRS1498145 GSM2197830 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197830 GEO Accession GSM2197830 SRX1838939 GSM2197831 SRP076476 SRS1498146 GSM2197831 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197831 GEO Accession GSM2197831 SRX1838940 GSM2197832 SRP076476 SRS1498147 GSM2197832 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197832 GEO Accession GSM2197832 SRX1838941 GSM2197833 SRP076476 SRS1498148 GSM2197833 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197833 GEO Accession GSM2197833 SRX1838942 GSM2197834 SRP076476 SRS1498149 GSM2197834 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197834 GEO Accession GSM2197834 SRX1838943 GSM2197835 SRP076476 SRS1498150 GSM2197835 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197835 GEO Accession GSM2197835 SRX1838944 GSM2197836 SRP076476 SRS1498151 GSM2197836 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197836 GEO Accession GSM2197836 SRX1838945 GSM2197837 SRP076476 SRS1498152 GSM2197837 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197837 GEO Accession GSM2197837 SRX1838946 GSM2197838 SRP076476 SRS1498153 GSM2197838 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197838 GEO Accession GSM2197838 SRX1838947 GSM2197839 SRP076476 SRS1498154 GSM2197839 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197839 GEO Accession GSM2197839 SRX1838948 GSM2197840 SRP076476 SRS1498156 GSM2197840 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197840 GEO Accession GSM2197840 SRX1838949 GSM2197841 SRP076476 SRS1498155 GSM2197841 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197841 GEO Accession GSM2197841 SRX1838950 GSM2197842 SRP076476 SRS1498157 GSM2197842 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197842 GEO Accession GSM2197842 SRX1838951 GSM2197843 SRP076476 SRS1498158 GSM2197843 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197843 GEO Accession GSM2197843 SRX1838952 GSM2197844 SRP076476 SRS1498159 GSM2197844 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197844 GEO Accession GSM2197844 SRX1838953 GSM2197845 SRP076476 SRS1498160 GSM2197845 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197845 GEO Accession GSM2197845 SRX1838954 GSM2197846 SRP076476 SRS1498161 GSM2197846 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197846 GEO Accession GSM2197846 SRX1838955 GSM2197847 SRP076476 SRS1498162 GSM2197847 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197847 GEO Accession GSM2197847 SRX1838956 GSM2197848 SRP076476 SRS1498163 GSM2197848 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197848 GEO Accession GSM2197848 SRX1838957 GSM2197849 SRP076476 SRS1498164 GSM2197849 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197849 GEO Accession GSM2197849 SRX1838958 GSM2197850 SRP076476 SRS1498165 GSM2197850 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197850 GEO Accession GSM2197850 SRX1838959 GSM2197851 SRP076476 SRS1498166 GSM2197851 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197851 GEO Accession GSM2197851 SRX1838960 GSM2197852 SRP076476 SRS1498167 GSM2197852 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197852 GEO Accession GSM2197852 SRX1838961 GSM2197853 SRP076476 SRS1498168 GSM2197853 ChIP-Seq GENOMIC ChIP All samples, including input, were processed for library construction for Illumina sequencing using Illumina’s TruSeq ChIP Sample Preparation Kit (Illumina cat# IP-202- 1012). In brief, DNA fragments were repaired to generate blunt ends, purified using Agencourt AMPure XP Beads (Beckman Coulter cat# A63881), and a single “A” nucleotide was added to each end. Double-stranded Illumina adaptors were ligated to the fragments. Ligation products were purified using Agencourt AMPure XP Beads, and subject to size selection using SPRIselect Beads (Beckman Coulter cat# B23318)in which both a left side size selection was performed at 0.9x volume, and a right side size selection was performed at 0.6x volume according to manufacturer’s specifications. Library fragments were then amplified for 16 cycles of PCR and products were purified using Agencourt AMPure XP Beads. Constructed libraries were run on the Agilent Bioananlyzer 2100 (Agilent Technologies) using either the DNA 7500 kit (cat# 5067-1504) or the High Sensitivity DNA kit (cat# 5067-4626) as appropriate to determine the average size and confirm the absence of unligated adaptors. The mean library size is approximately 330 bp. The ChIP-seq libraries were quantitated by qPCR using the Kapa SYBR FAST Universal kit (Kapa Biosystems) according to the Illumina’s Sequencing Library qPCR Quantification Guide. Libraries were multiplexed and sequenced on the Illumina HiSeq 2000 using Illumina’s kits and reagents as appropriate. We sequenced 3 biological replicates for the 0min, 60min, 90min, 180min, and 360min time points; two biological replicates for 240min time point; and one replicate for 40min time point. Illumina HiSeq 2000 gds 302197853 GEO Accession GSM2197853