SRX18501618 GSM6792800_r1 SRP411462 PRJNA908875 SRS15972233 GSM6792800 GSM6792800 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501619 GSM6792801_r1 SRP411462 PRJNA908875 SRS15972234 GSM6792801 GSM6792801 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501620 GSM6792802_r1 SRP411462 PRJNA908875 SRS15972235 GSM6792802 GSM6792802 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501621 GSM6792803_r1 SRP411462 PRJNA908875 SRS15972236 GSM6792803 GSM6792803 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501622 GSM6792804_r1 SRP411462 PRJNA908875 SRS15972237 GSM6792804 GSM6792804 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501623 GSM6792805_r1 SRP411462 PRJNA908875 SRS15972238 GSM6792805 GSM6792805 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501624 GSM6792806_r1 SRP411462 PRJNA908875 SRS15972239 GSM6792806 GSM6792806 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501625 GSM6792807_r1 SRP411462 PRJNA908875 SRS15972240 GSM6792807 GSM6792807 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501626 GSM6792808_r1 SRP411462 PRJNA908875 SRS15972241 GSM6792808 GSM6792808 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501627 GSM6792809_r1 SRP411462 PRJNA908875 SRS15972242 GSM6792809 GSM6792809 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501628 GSM6792810_r1 SRP411462 PRJNA908875 SRS15972243 GSM6792810 GSM6792810 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501629 GSM6792811_r1 SRP411462 PRJNA908875 SRS15972244 GSM6792811 GSM6792811 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501630 GSM6792812_r1 SRP411462 PRJNA908875 SRS15972245 GSM6792812 GSM6792812 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501631 GSM6792813_r1 SRP411462 PRJNA908875 SRS15972246 GSM6792813 GSM6792813 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501632 GSM6792814_r1 SRP411462 PRJNA908875 SRS15972247 GSM6792814 GSM6792814 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501633 GSM6792815_r1 SRP411462 PRJNA908875 SRS15972248 GSM6792815 GSM6792815 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501634 GSM6792816_r1 SRP411462 PRJNA908875 SRS15972249 GSM6792816 GSM6792816 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500 SRX18501635 GSM6792817_r1 SRP411462 PRJNA908875 SRS15972250 GSM6792817 GSM6792817 RNA-Seq TRANSCRIPTOMIC cDNA The tissue was homogenized by Bead crushers with 3.0 mm stainless beads and total ribonucleic acid (RNA) was extracted from tissues using a NucleoSpin RNA kit (Takara Bio, Japan) according to the manufacturer's instructions. The cDNA library generated by PCR amplification was examined using a Bioanalyzer 2100 system (Agilent Technologies, Inc., Santa Clara, USA) for quality control and sequenced with BGIseq-500. BGISEQ-500