SRX22330617 GSM7876456_r1 SRP429339 PRJNA948822 SRS19380505 GSM7876456 GSM7876456 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330618 GSM7876457_r1 SRP429339 PRJNA948822 SRS19380506 GSM7876457 GSM7876457 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330619 GSM7876458_r1 SRP429339 PRJNA948822 SRS19380507 GSM7876458 GSM7876458 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330620 GSM7876459_r1 SRP429339 PRJNA948822 SRS19380508 GSM7876459 GSM7876459 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330621 GSM7876460_r1 SRP429339 PRJNA948822 SRS19380509 GSM7876460 GSM7876460 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330622 GSM7876461_r1 SRP429339 PRJNA948822 SRS19380510 GSM7876461 GSM7876461 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330623 GSM7876462_r1 SRP429339 PRJNA948822 SRS19380511 GSM7876462 GSM7876462 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330624 GSM7876463_r1 SRP429339 PRJNA948822 SRS19380512 GSM7876463 GSM7876463 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330625 GSM7876464_r1 SRP429339 PRJNA948822 SRS19380513 GSM7876464 GSM7876464 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330626 GSM7876465_r1 SRP429339 PRJNA948822 SRS19380514 GSM7876465 GSM7876465 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330627 GSM7876466_r1 SRP429339 PRJNA948822 SRS19380515 GSM7876466 GSM7876466 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330628 GSM7876467_r1 SRP429339 PRJNA948822 SRS19380516 GSM7876467 GSM7876467 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330629 GSM7876468_r1 SRP429339 PRJNA948822 SRS19380518 GSM7876468 GSM7876468 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330630 GSM7876469_r1 SRP429339 PRJNA948822 SRS19380517 GSM7876469 GSM7876469 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330631 GSM7876470_r1 SRP429339 PRJNA948822 SRS19380519 GSM7876470 GSM7876470 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330632 GSM7876471_r1 SRP429339 PRJNA948822 SRS19380520 GSM7876471 GSM7876471 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330633 GSM7876472_r1 SRP429339 PRJNA948822 SRS19380521 GSM7876472 GSM7876472 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330634 GSM7876473_r1 SRP429339 PRJNA948822 SRS19380522 GSM7876473 GSM7876473 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330635 GSM7876474_r1 SRP429339 PRJNA948822 SRS19380523 GSM7876474 GSM7876474 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000 SRX22330636 GSM7876475_r1 SRP429339 PRJNA948822 SRS19380524 GSM7876475 GSM7876475 OTHER GENOMIC other Cells were fixed with 1% formaldehyde for 1 minute. After quenching and permeabilization, cells were treated with respective antibodies Samples were treated with pA/G-Mnase to cleave target DNA sequences following antibody incubation CUT&RUN libraries were prepared using NEBNext DNA Ultra II Library Prep kit according to manufacturer instructions. Libraries were amplified for 15 cycles in the thermo cycler and samples purified with magnetic purification beads (NEB E7104S) Illumina NovaSeq 6000