SRX2033491 GSM2283399 SRP082366 SRS1627436 GSM2283399 OTHER GENOMIC other 50.000 iNKT cells were sorted, washed once with PBS and lysed in 100 ul of ice cold lysis buffer (10 mM Tris-HCl, pH 7.4, 10 mM NaCl, 3mM MgCl2 and 0.1% IGEPAL CA-630). Then, nuclei were spun at 500g for 10 min and the pellet was resuspended in 50 ul transposase reaction mix [2.5 ul transposase (Illumina), 25 ul 2x TD buffer (Illumina) and 22.5 nuclease free water). The reaction was incubated for 30 minutes at 37. Samples were purified using MinElute kit (Qiagen). The purified DNA was amplified using Kapa Real time library amplification kit (Kapa Biosystems). Libraries were amplified for 10-11 cycles. Illumina HiSeq 2500 gds 302283399 GEO Accession GSM2283399 SRX2033492 GSM2283400 SRP082366 SRS1627435 GSM2283400 OTHER GENOMIC other 50.000 iNKT cells were sorted, washed once with PBS and lysed in 100 ul of ice cold lysis buffer (10 mM Tris-HCl, pH 7.4, 10 mM NaCl, 3mM MgCl2 and 0.1% IGEPAL CA-630). Then, nuclei were spun at 500g for 10 min and the pellet was resuspended in 50 ul transposase reaction mix [2.5 ul transposase (Illumina), 25 ul 2x TD buffer (Illumina) and 22.5 nuclease free water). The reaction was incubated for 30 minutes at 37. Samples were purified using MinElute kit (Qiagen). The purified DNA was amplified using Kapa Real time library amplification kit (Kapa Biosystems). Libraries were amplified for 10-11 cycles. Illumina HiSeq 2500 gds 302283400 GEO Accession GSM2283400 SRX2033493 GSM2283401 SRP082366 SRS1627437 GSM2283401 OTHER GENOMIC other 50.000 iNKT cells were sorted, washed once with PBS and lysed in 100 ul of ice cold lysis buffer (10 mM Tris-HCl, pH 7.4, 10 mM NaCl, 3mM MgCl2 and 0.1% IGEPAL CA-630). Then, nuclei were spun at 500g for 10 min and the pellet was resuspended in 50 ul transposase reaction mix [2.5 ul transposase (Illumina), 25 ul 2x TD buffer (Illumina) and 22.5 nuclease free water). The reaction was incubated for 30 minutes at 37. Samples were purified using MinElute kit (Qiagen). The purified DNA was amplified using Kapa Real time library amplification kit (Kapa Biosystems). Libraries were amplified for 10-11 cycles. Illumina HiSeq 2500 gds 302283401 GEO Accession GSM2283401 SRX2033494 GSM2283402 SRP082366 SRS1627438 GSM2283402 OTHER GENOMIC other 50.000 iNKT cells were sorted, washed once with PBS and lysed in 100 ul of ice cold lysis buffer (10 mM Tris-HCl, pH 7.4, 10 mM NaCl, 3mM MgCl2 and 0.1% IGEPAL CA-630). Then, nuclei were spun at 500g for 10 min and the pellet was resuspended in 50 ul transposase reaction mix [2.5 ul transposase (Illumina), 25 ul 2x TD buffer (Illumina) and 22.5 nuclease free water). The reaction was incubated for 30 minutes at 37. Samples were purified using MinElute kit (Qiagen). The purified DNA was amplified using Kapa Real time library amplification kit (Kapa Biosystems). Libraries were amplified for 10-11 cycles. Illumina HiSeq 2500 gds 302283402 GEO Accession GSM2283402 SRX2033495 GSM2283403 SRP082366 SRS1627439 GSM2283403 OTHER GENOMIC other 50.000 iNKT cells were sorted, washed once with PBS and lysed in 100 ul of ice cold lysis buffer (10 mM Tris-HCl, pH 7.4, 10 mM NaCl, 3mM MgCl2 and 0.1% IGEPAL CA-630). Then, nuclei were spun at 500g for 10 min and the pellet was resuspended in 50 ul transposase reaction mix [2.5 ul transposase (Illumina), 25 ul 2x TD buffer (Illumina) and 22.5 nuclease free water). The reaction was incubated for 30 minutes at 37. Samples were purified using MinElute kit (Qiagen). The purified DNA was amplified using Kapa Real time library amplification kit (Kapa Biosystems). Libraries were amplified for 10-11 cycles. Illumina HiSeq 2500 gds 302283403 GEO Accession GSM2283403 SRX2033496 GSM2283404 SRP082366 SRS1627440 GSM2283404 OTHER GENOMIC other 50.000 iNKT cells were sorted, washed once with PBS and lysed in 100 ul of ice cold lysis buffer (10 mM Tris-HCl, pH 7.4, 10 mM NaCl, 3mM MgCl2 and 0.1% IGEPAL CA-630). Then, nuclei were spun at 500g for 10 min and the pellet was resuspended in 50 ul transposase reaction mix [2.5 ul transposase (Illumina), 25 ul 2x TD buffer (Illumina) and 22.5 nuclease free water). The reaction was incubated for 30 minutes at 37. Samples were purified using MinElute kit (Qiagen). The purified DNA was amplified using Kapa Real time library amplification kit (Kapa Biosystems). Libraries were amplified for 10-11 cycles. Illumina HiSeq 2500 gds 302283404 GEO Accession GSM2283404