SRX5803315 GSM3755251 SRP196147 SRS4732995 GSM3755251 ChIP-Seq GENOMIC ChIP Mouse hair follicle stem cells were FACS-purified from CD1 WT mice at postnatal day 21. Lysates were clarified from sonicated nuclei and histone-DNA complexes were isolated with antibody. Libraries were prepared according to a ChIPmentation protocol (Schmidl et. al., Nature Methods, 2015 ). Briefly, immunoprecitiated nucleosomes on beads were tagmented by Tagmentation enzyme from the Nextera DNA Sample Prep Kit (Illumina). Follwoing tagmentation, the beads were washed and DNA elution, reerse cross-linking, DNA purification, and PCR amplification were performed. During PCR amplification, each sample were barcoded by different adaptor primers for illumina sequencing. Sequencing libraries were pooled and sequenced on the NextSeq 500 instrument with 37/38 cycles paried end high-output mode. NextSeq 500 gds 303755251 GSM3755251 SRX5803316 GSM3755252 SRP196147 SRS4732996 GSM3755252 ChIP-Seq GENOMIC ChIP Mouse hair follicle stem cells were FACS-purified from CD1 WT mice at postnatal day 21. Lysates were clarified from sonicated nuclei and histone-DNA complexes were isolated with antibody. Libraries were prepared according to a ChIPmentation protocol (Schmidl et. al., Nature Methods, 2015 ). Briefly, immunoprecitiated nucleosomes on beads were tagmented by Tagmentation enzyme from the Nextera DNA Sample Prep Kit (Illumina). Follwoing tagmentation, the beads were washed and DNA elution, reerse cross-linking, DNA purification, and PCR amplification were performed. During PCR amplification, each sample were barcoded by different adaptor primers for illumina sequencing. Sequencing libraries were pooled and sequenced on the NextSeq 500 instrument with 37/38 cycles paried end high-output mode. NextSeq 500 gds 303755252 GSM3755252 SRX5803317 GSM3755253 SRP196147 SRS4732997 GSM3755253 ChIP-Seq GENOMIC ChIP Mouse hair follicle stem cells were FACS-purified from CD1 WT mice at postnatal day 21. Lysates were clarified from sonicated nuclei and histone-DNA complexes were isolated with antibody. Libraries were prepared according to a ChIPmentation protocol (Schmidl et. al., Nature Methods, 2015 ). Briefly, immunoprecitiated nucleosomes on beads were tagmented by Tagmentation enzyme from the Nextera DNA Sample Prep Kit (Illumina). Follwoing tagmentation, the beads were washed and DNA elution, reerse cross-linking, DNA purification, and PCR amplification were performed. During PCR amplification, each sample were barcoded by different adaptor primers for illumina sequencing. Sequencing libraries were pooled and sequenced on the NextSeq 500 instrument with 37/38 cycles paried end high-output mode. NextSeq 500 gds 303755253 GSM3755253