SRX18016347 GSM6678874_r1 SRP404471 PRJNA894185 SRS15524332 GSM6678874 GSM6678874 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016348 GSM6678875_r1 SRP404471 PRJNA894185 SRS15524331 GSM6678875 GSM6678875 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016349 GSM6678876_r1 SRP404471 PRJNA894185 SRS15524333 GSM6678876 GSM6678876 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016350 GSM6678877_r1 SRP404471 PRJNA894185 SRS15524334 GSM6678877 GSM6678877 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016351 GSM6678878_r1 SRP404471 PRJNA894185 SRS15524335 GSM6678878 GSM6678878 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016352 GSM6678879_r1 SRP404471 PRJNA894185 SRS15524336 GSM6678879 GSM6678879 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016353 GSM6678880_r1 SRP404471 PRJNA894185 SRS15524337 GSM6678880 GSM6678880 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016354 GSM6678881_r1 SRP404471 PRJNA894185 SRS15524338 GSM6678881 GSM6678881 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016355 GSM6678882_r1 SRP404471 PRJNA894185 SRS15524339 GSM6678882 GSM6678882 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016356 GSM6678883_r1 SRP404471 PRJNA894185 SRS15524340 GSM6678883 GSM6678883 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016357 GSM6678884_r1 SRP404471 PRJNA894185 SRS15524341 GSM6678884 GSM6678884 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016358 GSM6678885_r1 SRP404471 PRJNA894185 SRS15524343 GSM6678885 GSM6678885 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016359 GSM6678886_r1 SRP404471 PRJNA894185 SRS15524342 GSM6678886 GSM6678886 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016360 GSM6678887_r1 SRP404471 PRJNA894185 SRS15524344 GSM6678887 GSM6678887 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016361 GSM6678888_r1 SRP404471 PRJNA894185 SRS15524345 GSM6678888 GSM6678888 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016362 GSM6678889_r1 SRP404471 PRJNA894185 SRS15524346 GSM6678889 GSM6678889 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016363 GSM6678890_r1 SRP404471 PRJNA894185 SRS15524347 GSM6678890 GSM6678890 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016364 GSM6678891_r1 SRP404471 PRJNA894185 SRS15524348 GSM6678891 GSM6678891 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016365 GSM6678892_r1 SRP404471 PRJNA894185 SRS15524349 GSM6678892 GSM6678892 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016366 GSM6678893_r1 SRP404471 PRJNA894185 SRS15524350 GSM6678893 GSM6678893 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016367 GSM6678894_r1 SRP404471 PRJNA894185 SRS15524351 GSM6678894 GSM6678894 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016368 GSM6678895_r1 SRP404471 PRJNA894185 SRS15524352 GSM6678895 GSM6678895 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016369 GSM6678896_r1 SRP404471 PRJNA894185 SRS15524353 GSM6678896 GSM6678896 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016370 GSM6678897_r1 SRP404471 PRJNA894185 SRS15524354 GSM6678897 GSM6678897 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016371 GSM6678898_r1 SRP404471 PRJNA894185 SRS15524355 GSM6678898 GSM6678898 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016372 GSM6678899_r1 SRP404471 PRJNA894185 SRS15524356 GSM6678899 GSM6678899 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016373 GSM6678900_r1 SRP404471 PRJNA894185 SRS15524357 GSM6678900 GSM6678900 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016374 GSM6678901_r1 SRP404471 PRJNA894185 SRS15524358 GSM6678901 GSM6678901 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016375 GSM6678902_r1 SRP404471 PRJNA894185 SRS15524359 GSM6678902 GSM6678902 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016376 GSM6678903_r1 SRP404471 PRJNA894185 SRS15524360 GSM6678903 GSM6678903 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016377 GSM6678904_r1 SRP404471 PRJNA894185 SRS15524361 GSM6678904 GSM6678904 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016378 GSM6678905_r1 SRP404471 PRJNA894185 SRS15524362 GSM6678905 GSM6678905 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016379 GSM6678906_r1 SRP404471 PRJNA894185 SRS15524363 GSM6678906 GSM6678906 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016380 GSM6678907_r1 SRP404471 PRJNA894185 SRS15524364 GSM6678907 GSM6678907 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016381 GSM6678908_r1 SRP404471 PRJNA894185 SRS15524365 GSM6678908 GSM6678908 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016382 GSM6678909_r1 SRP404471 PRJNA894185 SRS15524366 GSM6678909 GSM6678909 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016383 GSM6678910_r1 SRP404471 PRJNA894185 SRS15524367 GSM6678910 GSM6678910 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016384 GSM6678911_r1 SRP404471 PRJNA894185 SRS15524369 GSM6678911 GSM6678911 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016385 GSM6678912_r1 SRP404471 PRJNA894185 SRS15524368 GSM6678912 GSM6678912 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500 SRX18016386 GSM6678913_r1 SRP404471 PRJNA894185 SRS15524370 GSM6678913 GSM6678913 RNA-Seq TRANSCRIPTOMIC cDNA Cells were lysed in quanidine-isothiocyanate buffer and RNA was isolated using the RNeasy Fibrous Tissue Mini Kit according to manufacturer's instructions. Prior to library preparation, the quality of RNA was assessed with Bioanalyzer (Agilent technologies). mRNA libraries were generated by BGI and bulk RNA sequencing was performed using BGISEQ BGISEQ-500