SRX4328949 GSM3239769 SRP105340 PRJNA384573 SRS3490996 GSM3239769 ChIP-Seq GENOMIC ChIP Chromatins were cross-linked by 1% formaldehyde and extracted using EZ-ChIP Chromatin Immunoprecipitation kit (Millipore, 17-371). The chromatin was then sonicated to an average DNA fragment length of 100-500 bp on Covaris S2 . Sequencing libraries were generated, according to the manufacturer's instructions. Briefly, 4 ng of ChIP product was used for each library preparation. The NEBNext® Ultra™ II DNA Library Prep Kit for Illumina (E7645) was used to ligate adapters and for barcoding and amplification. Libraries was purified using SPRIselect® Reagent magnetic beads (Beckman Coulter, Inc. #B23317), quality-controlled by the Bioanalyzer, and quantified by qPCR. NextSeq 550 gds 303239769 GSM3239769 GEO Accession GSM3239769 SRX4328950 GSM3239770 SRP105340 PRJNA384573 SRS3490997 GSM3239770 ChIP-Seq GENOMIC ChIP Chromatins were cross-linked by 1% formaldehyde and extracted using EZ-ChIP Chromatin Immunoprecipitation kit (Millipore, 17-371). The chromatin was then sonicated to an average DNA fragment length of 100-500 bp on Covaris S2 . Sequencing libraries were generated, according to the manufacturer's instructions. Briefly, 4 ng of ChIP product was used for each library preparation. The NEBNext® Ultra™ II DNA Library Prep Kit for Illumina (E7645) was used to ligate adapters and for barcoding and amplification. Libraries was purified using SPRIselect® Reagent magnetic beads (Beckman Coulter, Inc. #B23317), quality-controlled by the Bioanalyzer, and quantified by qPCR. NextSeq 550 gds 303239770 GSM3239770 GEO Accession GSM3239770 SRX4328951 GSM3239771 SRP105340 PRJNA384573 SRS3490998 GSM3239771 ChIP-Seq GENOMIC ChIP Chromatins were cross-linked by 1% formaldehyde and extracted using EZ-ChIP Chromatin Immunoprecipitation kit (Millipore, 17-371). The chromatin was then sonicated to an average DNA fragment length of 100-500 bp on Covaris S2 . Sequencing libraries were generated, according to the manufacturer's instructions. Briefly, 4 ng of ChIP product was used for each library preparation. The NEBNext® Ultra™ II DNA Library Prep Kit for Illumina (E7645) was used to ligate adapters and for barcoding and amplification. Libraries was purified using SPRIselect® Reagent magnetic beads (Beckman Coulter, Inc. #B23317), quality-controlled by the Bioanalyzer, and quantified by qPCR. NextSeq 550 gds 303239771 GSM3239771 GEO Accession GSM3239771 SRX4328952 GSM3239772 SRP105340 PRJNA384573 SRS3490999 GSM3239772 ChIP-Seq GENOMIC ChIP Chromatins were cross-linked by 1% formaldehyde and extracted using EZ-ChIP Chromatin Immunoprecipitation kit (Millipore, 17-371). The chromatin was then sonicated to an average DNA fragment length of 100-500 bp on Covaris S2 . Sequencing libraries were generated, according to the manufacturer's instructions. Briefly, 4 ng of ChIP product was used for each library preparation. The NEBNext® Ultra™ II DNA Library Prep Kit for Illumina (E7645) was used to ligate adapters and for barcoding and amplification. Libraries was purified using SPRIselect® Reagent magnetic beads (Beckman Coulter, Inc. #B23317), quality-controlled by the Bioanalyzer, and quantified by qPCR. NextSeq 550 gds 303239772 GSM3239772 GEO Accession GSM3239772 SRX4328953 GSM3239773 SRP105340 PRJNA384573 SRS3491000 GSM3239773 ChIP-Seq GENOMIC ChIP Chromatins were cross-linked by 1% formaldehyde and extracted using EZ-ChIP Chromatin Immunoprecipitation kit (Millipore, 17-371). The chromatin was then sonicated to an average DNA fragment length of 100-500 bp on Covaris S2 . Sequencing libraries were generated, according to the manufacturer's instructions. Briefly, 4 ng of ChIP product was used for each library preparation. The NEBNext® Ultra™ II DNA Library Prep Kit for Illumina (E7645) was used to ligate adapters and for barcoding and amplification. Libraries was purified using SPRIselect® Reagent magnetic beads (Beckman Coulter, Inc. #B23317), quality-controlled by the Bioanalyzer, and quantified by qPCR. NextSeq 550 gds 303239773 GSM3239773 GEO Accession GSM3239773 SRX4328954 GSM3239774 SRP105340 PRJNA384573 SRS3491001 GSM3239774 ChIP-Seq GENOMIC ChIP Chromatins were cross-linked by 1% formaldehyde and extracted using EZ-ChIP Chromatin Immunoprecipitation kit (Millipore, 17-371). The chromatin was then sonicated to an average DNA fragment length of 100-500 bp on Covaris S2 . Sequencing libraries were generated, according to the manufacturer's instructions. Briefly, 4 ng of ChIP product was used for each library preparation. The NEBNext® Ultra™ II DNA Library Prep Kit for Illumina (E7645) was used to ligate adapters and for barcoding and amplification. Libraries was purified using SPRIselect® Reagent magnetic beads (Beckman Coulter, Inc. #B23317), quality-controlled by the Bioanalyzer, and quantified by qPCR. NextSeq 550 gds 303239774 GSM3239774 GEO Accession GSM3239774 SRX4328955 GSM3239775 SRP105340 PRJNA384573 SRS3491002 GSM3239775 ChIP-Seq GENOMIC ChIP Chromatins were cross-linked by 1% formaldehyde and extracted using EZ-ChIP Chromatin Immunoprecipitation kit (Millipore, 17-371). The chromatin was then sonicated to an average DNA fragment length of 100-500 bp on Covaris S2 . Sequencing libraries were generated, according to the manufacturer's instructions. Briefly, 4 ng of ChIP product was used for each library preparation. The NEBNext® Ultra™ II DNA Library Prep Kit for Illumina (E7645) was used to ligate adapters and for barcoding and amplification. Libraries was purified using SPRIselect® Reagent magnetic beads (Beckman Coulter, Inc. #B23317), quality-controlled by the Bioanalyzer, and quantified by qPCR. NextSeq 550 gds 303239775 GSM3239775 GEO Accession GSM3239775 SRX4328956 GSM3239776 SRP105340 PRJNA384573 SRS3491003 GSM3239776 ChIP-Seq GENOMIC ChIP Chromatins were cross-linked by 1% formaldehyde and extracted using EZ-ChIP Chromatin Immunoprecipitation kit (Millipore, 17-371). The chromatin was then sonicated to an average DNA fragment length of 100-500 bp on Covaris S2 . Sequencing libraries were generated, according to the manufacturer's instructions. Briefly, 4 ng of ChIP product was used for each library preparation. The NEBNext® Ultra™ II DNA Library Prep Kit for Illumina (E7645) was used to ligate adapters and for barcoding and amplification. Libraries was purified using SPRIselect® Reagent magnetic beads (Beckman Coulter, Inc. #B23317), quality-controlled by the Bioanalyzer, and quantified by qPCR. NextSeq 550 gds 303239776 GSM3239776 GEO Accession GSM3239776 SRX4328957 GSM3239777 SRP105340 PRJNA384573 SRS3491004 GSM3239777 ChIP-Seq GENOMIC ChIP Chromatins were cross-linked by 1% formaldehyde and extracted using EZ-ChIP Chromatin Immunoprecipitation kit (Millipore, 17-371). The chromatin was then sonicated to an average DNA fragment length of 100-500 bp on Covaris S2 . Sequencing libraries were generated, according to the manufacturer's instructions. Briefly, 4 ng of ChIP product was used for each library preparation. The NEBNext® Ultra™ II DNA Library Prep Kit for Illumina (E7645) was used to ligate adapters and for barcoding and amplification. Libraries was purified using SPRIselect® Reagent magnetic beads (Beckman Coulter, Inc. #B23317), quality-controlled by the Bioanalyzer, and quantified by qPCR. NextSeq 550 gds 303239777 GSM3239777 GEO Accession GSM3239777 SRX4328958 GSM3239778 SRP105340 PRJNA384573 SRS3491005 GSM3239778 ChIP-Seq GENOMIC ChIP Chromatins were cross-linked by 1% formaldehyde and extracted using EZ-ChIP Chromatin Immunoprecipitation kit (Millipore, 17-371). The chromatin was then sonicated to an average DNA fragment length of 100-500 bp on Covaris S2 . Sequencing libraries were generated, according to the manufacturer's instructions. Briefly, 4 ng of ChIP product was used for each library preparation. The NEBNext® Ultra™ II DNA Library Prep Kit for Illumina (E7645) was used to ligate adapters and for barcoding and amplification. Libraries was purified using SPRIselect® Reagent magnetic beads (Beckman Coulter, Inc. #B23317), quality-controlled by the Bioanalyzer, and quantified by qPCR. NextSeq 550 gds 303239778 GSM3239778 GEO Accession GSM3239778 SRX4328959 GSM3239779 SRP105340 PRJNA384573 SRS3491006 GSM3239779 ChIP-Seq GENOMIC ChIP Chromatins were cross-linked by 1% formaldehyde and extracted using EZ-ChIP Chromatin Immunoprecipitation kit (Millipore, 17-371). The chromatin was then sonicated to an average DNA fragment length of 100-500 bp on Covaris S2 . Sequencing libraries were generated, according to the manufacturer's instructions. Briefly, 4 ng of ChIP product was used for each library preparation. The NEBNext® Ultra™ II DNA Library Prep Kit for Illumina (E7645) was used to ligate adapters and for barcoding and amplification. Libraries was purified using SPRIselect® Reagent magnetic beads (Beckman Coulter, Inc. #B23317), quality-controlled by the Bioanalyzer, and quantified by qPCR. NextSeq 550 gds 303239779 GSM3239779 GEO Accession GSM3239779 SRX4328960 GSM3239780 SRP105340 PRJNA384573 SRS3491007 GSM3239780 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239780 GSM3239780 GEO Accession GSM3239780 SRX4328961 GSM3239781 SRP105340 PRJNA384573 SRS3491008 GSM3239781 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239781 GSM3239781 GEO Accession GSM3239781 SRX4328962 GSM3239782 SRP105340 PRJNA384573 SRS3491009 GSM3239782 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239782 GSM3239782 GEO Accession GSM3239782 SRX4328963 GSM3239783 SRP105340 PRJNA384573 SRS3491010 GSM3239783 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239783 GSM3239783 GEO Accession GSM3239783 SRX4328964 GSM3239784 SRP105340 PRJNA384573 SRS3491011 GSM3239784 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239784 GSM3239784 GEO Accession GSM3239784 SRX4328965 GSM3239785 SRP105340 PRJNA384573 SRS3491012 GSM3239785 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239785 GSM3239785 GEO Accession GSM3239785 SRX4328966 GSM3239786 SRP105340 PRJNA384573 SRS3491013 GSM3239786 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239786 GSM3239786 GEO Accession GSM3239786 SRX4328967 GSM3239787 SRP105340 PRJNA384573 SRS3491014 GSM3239787 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239787 GSM3239787 GEO Accession GSM3239787 SRX4328968 GSM3239788 SRP105340 PRJNA384573 SRS3491015 GSM3239788 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239788 GSM3239788 GEO Accession GSM3239788 SRX4328969 GSM3239789 SRP105340 PRJNA384573 SRS3491016 GSM3239789 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239789 GSM3239789 GEO Accession GSM3239789 SRX4328970 GSM3239790 SRP105340 PRJNA384573 SRS3491017 GSM3239790 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239790 GSM3239790 GEO Accession GSM3239790 SRX4328971 GSM3239791 SRP105340 PRJNA384573 SRS3491018 GSM3239791 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239791 GSM3239791 GEO Accession GSM3239791 SRX4328972 GSM3239792 SRP105340 PRJNA384573 SRS3491019 GSM3239792 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239792 GSM3239792 GEO Accession GSM3239792 SRX4328973 GSM3239793 SRP105340 PRJNA384573 SRS3491020 GSM3239793 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239793 GSM3239793 GEO Accession GSM3239793 SRX4328974 GSM3239794 SRP105340 PRJNA384573 SRS3491021 GSM3239794 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239794 GSM3239794 GEO Accession GSM3239794 SRX4328975 GSM3239795 SRP105340 PRJNA384573 SRS3491022 GSM3239795 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239795 GSM3239795 GEO Accession GSM3239795 SRX4328976 GSM3239796 SRP105340 PRJNA384573 SRS3491023 GSM3239796 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239796 GSM3239796 GEO Accession GSM3239796 SRX4328977 GSM3239797 SRP105340 PRJNA384573 SRS3491024 GSM3239797 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239797 GSM3239797 GEO Accession GSM3239797 SRX4328978 GSM3239798 SRP105340 PRJNA384573 SRS3491025 GSM3239798 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239798 GSM3239798 GEO Accession GSM3239798 SRX4328979 GSM3239799 SRP105340 PRJNA384573 SRS3491026 GSM3239799 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239799 GSM3239799 GEO Accession GSM3239799 SRX4328980 GSM3239800 SRP105340 PRJNA384573 SRS3491027 GSM3239800 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239800 GSM3239800 GEO Accession GSM3239800 SRX4328981 GSM3239801 SRP105340 PRJNA384573 SRS3491028 GSM3239801 RNA-Seq TRANSCRIPTOMIC cDNA For cultured cells, total RNA was extracted with RNeasy Plus mini kit (Qiagen, 74136) with QiaShredder (Qiagen, 79656). For sorted cells, samples at the indicated time points were collected and lysed in TRIzolTM Reagent (Invitrogen, 15596026). Sequencing libraries were generated using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (#E7530L, NEB), according to the manufacturer's instructions. A total amount of 2µg RNA per sample was used as input material for library preparation. The library fragments were purified with QiaQuick PCR kits (Oiagen, 28106), quality-controlled by Bioanalyzer 2100 and quantified by qPCR. Illumina HiSeq 2500 gds 303239801 GSM3239801 GEO Accession GSM3239801