SRX5494947 GSM3660747 SRP187944 SRS4464607 GSM3660747 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660747 GSM3660747 GEO Accession GSM3660747 SRX5494948 GSM3660748 SRP187944 SRS4464608 GSM3660748 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660748 GSM3660748 GEO Accession GSM3660748 SRX5494949 GSM3660749 SRP187944 SRS4464610 GSM3660749 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660749 GSM3660749 GEO Accession GSM3660749 SRX5494950 GSM3660750 SRP187944 SRS4464609 GSM3660750 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660750 GSM3660750 GEO Accession GSM3660750 SRX5494951 GSM3660751 SRP187944 SRS4464611 GSM3660751 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660751 GSM3660751 GEO Accession GSM3660751 SRX5494952 GSM3660752 SRP187944 SRS4464612 GSM3660752 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660752 GSM3660752 GEO Accession GSM3660752 SRX5494953 GSM3660753 SRP187944 SRS4464613 GSM3660753 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660753 GSM3660753 GEO Accession GSM3660753 SRX5494954 GSM3660754 SRP187944 SRS4464614 GSM3660754 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660754 GSM3660754 GEO Accession GSM3660754 SRX5494955 GSM3660755 SRP187944 SRS4464615 GSM3660755 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660755 GSM3660755 GEO Accession GSM3660755 SRX5494956 GSM3660756 SRP187944 SRS4464617 GSM3660756 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660756 GSM3660756 GEO Accession GSM3660756 SRX5494957 GSM3660757 SRP187944 SRS4464616 GSM3660757 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660757 GSM3660757 GEO Accession GSM3660757 SRX5494958 GSM3660758 SRP187944 SRS4464618 GSM3660758 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660758 GSM3660758 GEO Accession GSM3660758 SRX5494959 GSM3660759 SRP187944 SRS4464619 GSM3660759 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660759 GSM3660759 GEO Accession GSM3660759 SRX5494960 GSM3660760 SRP187944 SRS4464620 GSM3660760 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660760 GSM3660760 GEO Accession GSM3660760 SRX5494961 GSM3660761 SRP187944 SRS4464621 GSM3660761 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660761 GSM3660761 GEO Accession GSM3660761 SRX5494962 GSM3660762 SRP187944 SRS4464622 GSM3660762 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660762 GSM3660762 GEO Accession GSM3660762 SRX5494963 GSM3660763 SRP187944 SRS4464623 GSM3660763 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660763 GSM3660763 GEO Accession GSM3660763 SRX5494964 GSM3660764 SRP187944 SRS4464624 GSM3660764 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660764 GSM3660764 GEO Accession GSM3660764 SRX5494965 GSM3660765 SRP187944 SRS4464625 GSM3660765 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660765 GSM3660765 GEO Accession GSM3660765 SRX5494966 GSM3660766 SRP187944 SRS4464626 GSM3660766 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660766 GSM3660766 GEO Accession GSM3660766 SRX5494967 GSM3660767 SRP187944 SRS4464628 GSM3660767 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660767 GSM3660767 GEO Accession GSM3660767 SRX5494968 GSM3660768 SRP187944 SRS4464627 GSM3660768 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660768 GSM3660768 GEO Accession GSM3660768 SRX5494969 GSM3660769 SRP187944 SRS4464629 GSM3660769 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660769 GSM3660769 GEO Accession GSM3660769 SRX5494970 GSM3660770 SRP187944 SRS4464630 GSM3660770 ChIP-Seq GENOMIC ChIP Preparation of chromatin samples and immunoprecipitation were performed as described previously (Gendrel et al., 2005). Three to four flower buds were used as one replicate. Cross-link was conducted as described previously (Saito et al., 2015) with minor modifications. In brief, each flower bud was first cut longitudinally by razor and divided into 8 equal parts. The immunoprecipitated chromatin samples were amplified and used for library construction using the ThruPLEX DNA-seq Kit (Takara Bio USA) as per the manufacturer's instructions. Illumina HiSeq 2000 gds 303660770 GSM3660770 GEO Accession GSM3660770