SRX1519419 GSM2028114 SRP068139 SRS1237853 GSM2028114 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from negative control, TBX3 and CAPERa KD HFFs using the nucleospin Kit (Clontech) according to the manufacturer's protocol Poly-A RNA was purified, fragmented, primed with random hexamers and used to generate first strand cDNA using reverse transcriptase. Samples that passed quality control steps were used for Illumina library preparation using the Illumina TruSeq RNA Sample Prep protocol Single-end 50 bp reads Illumina HiSeq 2000 gds 302028114 GEO Accession GSM2028114 SRX1519420 GSM2028115 SRP068139 SRS1237851 GSM2028115 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from negative control, TBX3 and CAPERa KD HFFs using the nucleospin Kit (Clontech) according to the manufacturer's protocol Poly-A RNA was purified, fragmented, primed with random hexamers and used to generate first strand cDNA using reverse transcriptase. Samples that passed quality control steps were used for Illumina library preparation using the Illumina TruSeq RNA Sample Prep protocol Single-end 50 bp reads Illumina HiSeq 2000 gds 302028115 GEO Accession GSM2028115 SRX1519421 GSM2028116 SRP068139 SRS1237850 GSM2028116 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from negative control, TBX3 and CAPERa KD HFFs using the nucleospin Kit (Clontech) according to the manufacturer's protocol Poly-A RNA was purified, fragmented, primed with random hexamers and used to generate first strand cDNA using reverse transcriptase. Samples that passed quality control steps were used for Illumina library preparation using the Illumina TruSeq RNA Sample Prep protocol Single-end 50 bp reads Illumina HiSeq 2000 gds 302028116 GEO Accession GSM2028116 SRX1519422 GSM2028117 SRP068139 SRS1237849 GSM2028117 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from negative control, TBX3 and CAPERa KD HFFs using the nucleospin Kit (Clontech) according to the manufacturer's protocol Poly-A RNA was purified, fragmented, primed with random hexamers and used to generate first strand cDNA using reverse transcriptase. Samples that passed quality control steps were used for Illumina library preparation using the Illumina TruSeq RNA Sample Prep protocol Single-end 50 bp reads Illumina HiSeq 2000 gds 302028117 GEO Accession GSM2028117 SRX1519423 GSM2028118 SRP068139 SRS1237848 GSM2028118 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from negative control, TBX3 and CAPERa KD HFFs using the nucleospin Kit (Clontech) according to the manufacturer's protocol Poly-A RNA was purified, fragmented, primed with random hexamers and used to generate first strand cDNA using reverse transcriptase. Samples that passed quality control steps were used for Illumina library preparation using the Illumina TruSeq RNA Sample Prep protocol Single-end 50 bp reads Illumina HiSeq 2000 gds 302028118 GEO Accession GSM2028118 SRX1519424 GSM2028119 SRP068139 SRS1237847 GSM2028119 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from negative control, TBX3 and CAPERa KD HFFs using the nucleospin Kit (Clontech) according to the manufacturer's protocol Poly-A RNA was purified, fragmented, primed with random hexamers and used to generate first strand cDNA using reverse transcriptase. Samples that passed quality control steps were used for Illumina library preparation using the Illumina TruSeq RNA Sample Prep protocol Single-end 50 bp reads Illumina HiSeq 2000 gds 302028119 GEO Accession GSM2028119 SRX1519425 GSM2028120 SRP068139 SRS1237846 GSM2028120 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from negative control, TBX3 and CAPERa KD HFFs using the nucleospin Kit (Clontech) according to the manufacturer's protocol Poly-A RNA was purified, fragmented, primed with random hexamers and used to generate first strand cDNA using reverse transcriptase. Samples that passed quality control steps were used for Illumina library preparation using the Illumina TruSeq RNA Sample Prep protocol Single-end 50 bp reads Illumina HiSeq 2000 gds 302028120 GEO Accession GSM2028120 SRX1519426 GSM2028121 SRP068139 SRS1237845 GSM2028121 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from negative control, TBX3 and CAPERa KD HFFs using the nucleospin Kit (Clontech) according to the manufacturer's protocol Poly-A RNA was purified, fragmented, primed with random hexamers and used to generate first strand cDNA using reverse transcriptase. Samples that passed quality control steps were used for Illumina library preparation using the Illumina TruSeq RNA Sample Prep protocol Single-end 50 bp reads Illumina HiSeq 2000 gds 302028121 GEO Accession GSM2028121 SRX1519427 GSM2028122 SRP068139 SRS1237844 GSM2028122 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from negative control, TBX3 and CAPERa KD HFFs using the nucleospin Kit (Clontech) according to the manufacturer's protocol Poly-A RNA was purified, fragmented, primed with random hexamers and used to generate first strand cDNA using reverse transcriptase. Samples that passed quality control steps were used for Illumina library preparation using the Illumina TruSeq RNA Sample Prep protocol Single-end 50 bp reads Illumina HiSeq 2000 gds 302028122 GEO Accession GSM2028122 SRX1519428 GSM2028123 SRP068139 SRS1237843 GSM2028123 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from negative control, TBX3 and CAPERa KD HFFs using the nucleospin Kit (Clontech) according to the manufacturer's protocol Poly-A RNA was purified, fragmented, primed with random hexamers and used to generate first strand cDNA using reverse transcriptase. Samples that passed quality control steps were used for Illumina library preparation using the Illumina TruSeq RNA Sample Prep protocol Single-end 50 bp reads Illumina HiSeq 2000 gds 302028123 GEO Accession GSM2028123