SRX18487378 GSM6784413_r1 SRP411261 PRJNA908252 SRS15960293 GSM6784413 GSM6784413 OTHER GENOMIC other Cells were allowed to grow to confluency and harvested. Equal number of cells for each category suspended in wash buffer and subjected to CutnRun assay according to Skene and Heinkoff 2018. 1ng CutnRun DNA was used to generate libraries using Kapa Hyper prep kit and SeqCapAdapter Kit A. 14 PCR cycles used to amplify the libraries. Ampure Xp beads used for library purification and fragment analysis done to check quality of the libraries made. Paired end 2X25 bp illumina Hi-seq sequencing performed. Illumina HiSeq 4000 SRX18487379 GSM6784414_r1 SRP411261 PRJNA908252 SRS15960294 GSM6784414 GSM6784414 OTHER GENOMIC other Cells were allowed to grow to confluency and harvested. Equal number of cells for each category suspended in wash buffer and subjected to CutnRun assay according to Skene and Heinkoff 2018. 1ng CutnRun DNA was used to generate libraries using Kapa Hyper prep kit and SeqCapAdapter Kit A. 14 PCR cycles used to amplify the libraries. Ampure Xp beads used for library purification and fragment analysis done to check quality of the libraries made. Paired end 2X25 bp illumina Hi-seq sequencing performed. Illumina HiSeq 4000 SRX18487380 GSM6784415_r1 SRP411261 PRJNA908252 SRS15960295 GSM6784415 GSM6784415 OTHER GENOMIC other Cells were allowed to grow to confluency and harvested. Equal number of cells for each category suspended in wash buffer and subjected to CutnRun assay according to Skene and Heinkoff 2018. 1ng CutnRun DNA was used to generate libraries using Kapa Hyper prep kit and SeqCapAdapter Kit A. 14 PCR cycles used to amplify the libraries. Ampure Xp beads used for library purification and fragment analysis done to check quality of the libraries made. Paired end 2X25 bp illumina Hi-seq sequencing performed. Illumina HiSeq 4000 SRX18487381 GSM6784416_r1 SRP411261 PRJNA908252 SRS15960296 GSM6784416 GSM6784416 OTHER GENOMIC other Cells were allowed to grow to confluency and harvested. Equal number of cells for each category suspended in wash buffer and subjected to CutnRun assay according to Skene and Heinkoff 2018. 1ng CutnRun DNA was used to generate libraries using Kapa Hyper prep kit and SeqCapAdapter Kit A. 14 PCR cycles used to amplify the libraries. Ampure Xp beads used for library purification and fragment analysis done to check quality of the libraries made. Paired end 2X25 bp illumina Hi-seq sequencing performed. Illumina HiSeq 4000 SRX18487382 GSM6784417_r1 SRP411261 PRJNA908252 SRS15960297 GSM6784417 GSM6784417 OTHER GENOMIC other Cells were allowed to grow to confluency and harvested. Equal number of cells for each category suspended in wash buffer and subjected to CutnRun assay according to Skene and Heinkoff 2018. 1ng CutnRun DNA was used to generate libraries using Kapa Hyper prep kit and SeqCapAdapter Kit A. 14 PCR cycles used to amplify the libraries. Ampure Xp beads used for library purification and fragment analysis done to check quality of the libraries made. Paired end 2X25 bp illumina Hi-seq sequencing performed. Illumina HiSeq 4000 SRX18487383 GSM6784418_r1 SRP411261 PRJNA908252 SRS15960298 GSM6784418 GSM6784418 OTHER GENOMIC other Cells were allowed to grow to confluency and harvested. Equal number of cells for each category suspended in wash buffer and subjected to CutnRun assay according to Skene and Heinkoff 2018. 1ng CutnRun DNA was used to generate libraries using Kapa Hyper prep kit and SeqCapAdapter Kit A. 14 PCR cycles used to amplify the libraries. Ampure Xp beads used for library purification and fragment analysis done to check quality of the libraries made. Paired end 2X25 bp illumina Hi-seq sequencing performed. Illumina HiSeq 4000 SRX18487384 GSM6784419_r1 SRP411261 PRJNA908252 SRS15960299 GSM6784419 GSM6784419 OTHER GENOMIC other Cells were allowed to grow to confluency and harvested. Equal number of cells for each category suspended in wash buffer and subjected to CutnRun assay according to Skene and Heinkoff 2018. 1ng CutnRun DNA was used to generate libraries using Kapa Hyper prep kit and SeqCapAdapter Kit A. 14 PCR cycles used to amplify the libraries. Ampure Xp beads used for library purification and fragment analysis done to check quality of the libraries made. Paired end 2X25 bp illumina Hi-seq sequencing performed. Illumina HiSeq 4000