SRX15104825 GSM6086736_r1 SRP373125 PRJNA834058 SRS12850065 GSM6086736 GSM6086736 RNA-Seq TRANSCRIPTOMIC cDNA HUVEC cells were grown until pass. 10 max in serum-reduced endothelial cell culture medium (Endopan 3). Cells were treated with Myeloperoxidase protein (MPO) in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15104826 GSM6086737_r1 SRP373125 PRJNA834058 SRS12850066 GSM6086737 GSM6086737 RNA-Seq TRANSCRIPTOMIC cDNA HUVEC cells were grown until pass. 10 max in serum-reduced endothelial cell culture medium (Endopan 3). Cells were treated with Myeloperoxidase protein (MPO) in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15104827 GSM6086738_r1 SRP373125 PRJNA834058 SRS12850067 GSM6086738 GSM6086738 RNA-Seq TRANSCRIPTOMIC cDNA HUVEC cells were grown until pass. 10 max in serum-reduced endothelial cell culture medium (Endopan 3). Cells were treated with Myeloperoxidase protein (MPO) in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15104828 GSM6086739_r1 SRP373125 PRJNA834058 SRS12850068 GSM6086739 GSM6086739 RNA-Seq TRANSCRIPTOMIC cDNA HUVEC cells were grown until pass. 10 max in serum-reduced endothelial cell culture medium (Endopan 3). Cells were treated with Myeloperoxidase protein (MPO) in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15104829 GSM6086740_r1 SRP373125 PRJNA834058 SRS12850069 GSM6086740 GSM6086740 RNA-Seq TRANSCRIPTOMIC cDNA HUVEC cells were grown until pass. 10 max in serum-reduced endothelial cell culture medium (Endopan 3). Cells were treated with Myeloperoxidase protein (MPO) in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15104830 GSM6086741_r1 SRP373125 PRJNA834058 SRS12850070 GSM6086741 GSM6086741 RNA-Seq TRANSCRIPTOMIC cDNA HUVEC cells were grown until pass. 10 max in serum-reduced endothelial cell culture medium (Endopan 3). Cells were treated with Myeloperoxidase protein (MPO) in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15104831 GSM6086742_r1 SRP373125 PRJNA834058 SRS12850071 GSM6086742 GSM6086742 RNA-Seq TRANSCRIPTOMIC cDNA HUVEC cells were grown until pass. 10 max in serum-reduced endothelial cell culture medium (Endopan 3). Cells were treated with Myeloperoxidase protein (MPO) in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15104832 GSM6086743_r1 SRP373125 PRJNA834058 SRS12850072 GSM6086743 GSM6086743 RNA-Seq TRANSCRIPTOMIC cDNA HUVEC cells were grown until pass. 10 max in serum-reduced endothelial cell culture medium (Endopan 3). Cells were treated with Myeloperoxidase protein (MPO) in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000