SRX1146021 GSM1853545 SRP062389 SRS1030669 GSM1853545 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853545 GEO Accession GSM1853545 SRX1146022 GSM1853551 SRP062389 SRS1030663 GSM1853551 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853551 GEO Accession GSM1853551 SRX1146023 GSM1853553 SRP062389 SRS1030664 GSM1853553 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853553 GEO Accession GSM1853553 SRX1146024 GSM1853555 SRP062389 SRS1030661 GSM1853555 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853555 GEO Accession GSM1853555 SRX1146025 GSM1853556 SRP062389 SRS1030660 GSM1853556 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853556 GEO Accession GSM1853556 SRX1146026 GSM1853558 SRP062389 SRS1030662 GSM1853558 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853558 GEO Accession GSM1853558 SRX1146027 GSM1853560 SRP062389 SRS1030659 GSM1853560 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853560 GEO Accession GSM1853560 SRX1146028 GSM1853561 SRP062389 SRS1030658 GSM1853561 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853561 GEO Accession GSM1853561 SRX1146029 GSM1853563 SRP062389 SRS1030656 GSM1853563 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853563 GEO Accession GSM1853563 SRX1146030 GSM1853565 SRP062389 SRS1030655 GSM1853565 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853565 GEO Accession GSM1853565 SRX1146031 GSM1853567 SRP062389 SRS1030657 GSM1853567 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853567 GEO Accession GSM1853567 SRX1146032 GSM1853568 SRP062389 SRS1030654 GSM1853568 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853568 GEO Accession GSM1853568 SRX1146033 GSM1853570 SRP062389 SRS1030653 GSM1853570 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853570 GEO Accession GSM1853570 SRX1146034 GSM1853572 SRP062389 SRS1030651 GSM1853572 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853572 GEO Accession GSM1853572 SRX1146035 GSM1853573 SRP062389 SRS1030650 GSM1853573 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853573 GEO Accession GSM1853573 SRX1146036 GSM1853575 SRP062389 SRS1030652 GSM1853575 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853575 GEO Accession GSM1853575 SRX1146037 GSM1853577 SRP062389 SRS1030648 GSM1853577 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853577 GEO Accession GSM1853577 SRX1146038 GSM1853578 SRP062389 SRS1030649 GSM1853578 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853578 GEO Accession GSM1853578 SRX1146039 GSM1853580 SRP062389 SRS1030646 GSM1853580 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853580 GEO Accession GSM1853580 SRX1146040 GSM1853582 SRP062389 SRS1030647 GSM1853582 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853582 GEO Accession GSM1853582 SRX1146041 GSM1853584 SRP062389 SRS1030644 GSM1853584 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853584 GEO Accession GSM1853584 SRX1146042 GSM1853586 SRP062389 SRS1030643 GSM1853586 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853586 GEO Accession GSM1853586 SRX1146043 GSM1853587 SRP062389 SRS1030642 GSM1853587 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853587 GEO Accession GSM1853587 SRX1146044 GSM1853589 SRP062389 SRS1030640 GSM1853589 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853589 GEO Accession GSM1853589 SRX1146045 GSM1853591 SRP062389 SRS1030641 GSM1853591 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853591 GEO Accession GSM1853591 SRX1146046 GSM1853593 SRP062389 SRS1030645 GSM1853593 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853593 GEO Accession GSM1853593 SRX1146047 GSM1853594 SRP062389 SRS1030639 GSM1853594 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853594 GEO Accession GSM1853594 SRX1146048 GSM1853596 SRP062389 SRS1030638 GSM1853596 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853596 GEO Accession GSM1853596 SRX1146049 GSM1853598 SRP062389 SRS1030637 GSM1853598 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853598 GEO Accession GSM1853598 SRX1146050 GSM1853600 SRP062389 SRS1030636 GSM1853600 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853600 GEO Accession GSM1853600 SRX1146051 GSM1853602 SRP062389 SRS1030634 GSM1853602 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853602 GEO Accession GSM1853602 SRX1146052 GSM1853603 SRP062389 SRS1030633 GSM1853603 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853603 GEO Accession GSM1853603 SRX1146053 GSM1853605 SRP062389 SRS1030635 GSM1853605 RNA-Seq TRANSCRIPTOMIC cDNA For RNAseq experiments, individual replicates were collected and extracted using the RNAqueous kit (Life Technologies #AM1912). DNase digestion was performed twice, once in batch and once on the column, using the RNAeasy kit (Qiagen #74104). RNA libraries were prepared for sequencing using standard ribo-depleted Illumina protocols. We sequenced using the Illumina HiSeq, outputting single end, 50 bp, stranded RNAseq reads Illumina HiSeq 2500 gds 301853605 GEO Accession GSM1853605