SRX5171512 GSM3525910 SRP174100 SRS4179134 GSM3525910 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525910 GSM3525910 GEO Accession GSM3525910 SRX5171513 GSM3525911 SRP174100 SRS4179135 GSM3525911 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525911 GSM3525911 GEO Accession GSM3525911 SRX5171514 GSM3525912 SRP174100 SRS4179136 GSM3525912 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525912 GSM3525912 GEO Accession GSM3525912 SRX5171515 GSM3525913 SRP174100 SRS4179137 GSM3525913 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525913 GSM3525913 GEO Accession GSM3525913 SRX5171516 GSM3525914 SRP174100 SRS4179138 GSM3525914 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525914 GSM3525914 GEO Accession GSM3525914 SRX5171517 GSM3525915 SRP174100 SRS4179139 GSM3525915 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525915 GSM3525915 GEO Accession GSM3525915 SRX5171518 GSM3525916 SRP174100 SRS4179140 GSM3525916 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525916 GSM3525916 GEO Accession GSM3525916 SRX5171519 GSM3525917 SRP174100 SRS4179141 GSM3525917 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525917 GSM3525917 GEO Accession GSM3525917 SRX5171520 GSM3525918 SRP174100 SRS4179142 GSM3525918 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525918 GSM3525918 GEO Accession GSM3525918 SRX5171521 GSM3525919 SRP174100 SRS4179143 GSM3525919 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525919 GSM3525919 GEO Accession GSM3525919 SRX5171522 GSM3525920 SRP174100 SRS4179144 GSM3525920 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525920 GSM3525920 GEO Accession GSM3525920 SRX5171523 GSM3525921 SRP174100 SRS4179145 GSM3525921 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525921 GSM3525921 GEO Accession GSM3525921 SRX5171524 GSM3525922 SRP174100 SRS4179146 GSM3525922 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525922 GSM3525922 GEO Accession GSM3525922 SRX5171525 GSM3525923 SRP174100 SRS4179147 GSM3525923 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525923 GSM3525923 GEO Accession GSM3525923 SRX5171526 GSM3525924 SRP174100 SRS4179148 GSM3525924 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525924 GSM3525924 GEO Accession GSM3525924 SRX5171527 GSM3525925 SRP174100 SRS4179149 GSM3525925 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525925 GSM3525925 GEO Accession GSM3525925 SRX5171528 GSM3525926 SRP174100 SRS4179150 GSM3525926 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525926 GSM3525926 GEO Accession GSM3525926 SRX5171529 GSM3525927 SRP174100 SRS4179151 GSM3525927 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525927 GSM3525927 GEO Accession GSM3525927 SRX5171530 GSM3525928 SRP174100 SRS4179152 GSM3525928 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525928 GSM3525928 GEO Accession GSM3525928 SRX5171531 GSM3525929 SRP174100 SRS4179153 GSM3525929 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525929 GSM3525929 GEO Accession GSM3525929 SRX5171532 GSM3525930 SRP174100 SRS4179154 GSM3525930 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525930 GSM3525930 GEO Accession GSM3525930 SRX5171533 GSM3525931 SRP174100 SRS4179155 GSM3525931 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525931 GSM3525931 GEO Accession GSM3525931 SRX5171534 GSM3525932 SRP174100 SRS4179156 GSM3525932 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525932 GSM3525932 GEO Accession GSM3525932 SRX5171535 GSM3525933 SRP174100 SRS4179157 GSM3525933 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525933 GSM3525933 GEO Accession GSM3525933 SRX5171536 GSM3525934 SRP174100 SRS4179158 GSM3525934 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525934 GSM3525934 GEO Accession GSM3525934 SRX5171537 GSM3525935 SRP174100 SRS4179159 GSM3525935 ATAC-seq GENOMIC other Samples for ATAC-seq analysis were prepared from CD14+-MACS-enriched monocytes from fresh PBMCs (Pan Monocyte Isolation Kit, Miltenyi Biotec). 50,000 cells were washed in cold PBS and resuspended in cold lysis buffer (10 mM NaCL, 3 mM MgCl2, 0.1 % IGEPAL, 10mM Tris-HCl pH7.4). After centrifugation, pellets were incubated in primer-loaded transposase Tn5 in reaction buffer (10 mM TAPS-NaOH (pH 8.5) at 25°C, 5 mM MgCl2, 10% DMF) for 30 min at 37ºC. Samples were subsequently immediately purified using the MinElute kit (Qiagen GmbH) according to the manufacturer's guidelines, eluted in 10 µl H2O and stored at -20 ºC until further processing. Illumina HiSeq 1500 gds 303525935 GSM3525935 GEO Accession GSM3525935