SRX22322339 GSM7874729_r1 SRP469515 PRJNA1034138 SRS19372950 GSM7874729 GSM7874729 ChIP-Seq GENOMIC ChIP Chromatin was extracted from isolated nuclei and sheared to 100-1000bp. Primary antibody was incubated overnight for ChIP reactions. Crosslinks were reversed by adding NaCl and heating at 65 °C for 15 h, RNase A was added and incubated for 2 h at 37 °C, and Proteinase K added and incubated 2 h at 63 °C. DNA was isolated using the MinElute PCR Purification Kit (Qiagen 28004). Libraries were made using NEBNext Ultra II Library Kit (E7645) and sequenced on an Illumina Nova Seq at a depth of 100 million paired end reads. Illumina NovaSeq 6000 SRX22322340 GSM7874730_r1 SRP469515 PRJNA1034138 SRS19372951 GSM7874730 GSM7874730 ChIP-Seq GENOMIC ChIP Chromatin was extracted from isolated nuclei and sheared to 100-1000bp. Primary antibody was incubated overnight for ChIP reactions. Crosslinks were reversed by adding NaCl and heating at 65 °C for 15 h, RNase A was added and incubated for 2 h at 37 °C, and Proteinase K added and incubated 2 h at 63 °C. DNA was isolated using the MinElute PCR Purification Kit (Qiagen 28004). Libraries were made using NEBNext Ultra II Library Kit (E7645) and sequenced on an Illumina Nova Seq at a depth of 100 million paired end reads. Illumina NovaSeq 6000 SRX22322341 GSM7874731_r1 SRP469515 PRJNA1034138 SRS19372952 GSM7874731 GSM7874731 ChIP-Seq GENOMIC ChIP Chromatin was extracted from isolated nuclei and sheared to 100-1000bp. Primary antibody was incubated overnight for ChIP reactions. Crosslinks were reversed by adding NaCl and heating at 65 °C for 15 h, RNase A was added and incubated for 2 h at 37 °C, and Proteinase K added and incubated 2 h at 63 °C. DNA was isolated using the MinElute PCR Purification Kit (Qiagen 28004). Libraries were made using NEBNext Ultra II Library Kit (E7645) and sequenced on an Illumina Nova Seq at a depth of 100 million paired end reads. Illumina NovaSeq 6000 SRX22322342 GSM7874732_r1 SRP469515 PRJNA1034138 SRS19372953 GSM7874732 GSM7874732 ChIP-Seq GENOMIC ChIP Chromatin was extracted from isolated nuclei and sheared to 100-1000bp. Primary antibody was incubated overnight for ChIP reactions. Crosslinks were reversed by adding NaCl and heating at 65 °C for 15 h, RNase A was added and incubated for 2 h at 37 °C, and Proteinase K added and incubated 2 h at 63 °C. DNA was isolated using the MinElute PCR Purification Kit (Qiagen 28004). Libraries were made using NEBNext Ultra II Library Kit (E7645) and sequenced on an Illumina Nova Seq at a depth of 100 million paired end reads. Illumina NovaSeq 6000 SRX22322343 GSM7874733_r1 SRP469515 PRJNA1034138 SRS19372954 GSM7874733 GSM7874733 ChIP-Seq GENOMIC ChIP Chromatin was extracted from isolated nuclei and sheared to 100-1000bp. Primary antibody was incubated overnight for ChIP reactions. Crosslinks were reversed by adding NaCl and heating at 65 °C for 15 h, RNase A was added and incubated for 2 h at 37 °C, and Proteinase K added and incubated 2 h at 63 °C. DNA was isolated using the MinElute PCR Purification Kit (Qiagen 28004). Libraries were made using NEBNext Ultra II Library Kit (E7645) and sequenced on an Illumina Nova Seq at a depth of 100 million paired end reads. Illumina NovaSeq 6000 SRX22322344 GSM7874734_r1 SRP469515 PRJNA1034138 SRS19372955 GSM7874734 GSM7874734 ChIP-Seq GENOMIC ChIP Chromatin was extracted from isolated nuclei and sheared to 100-1000bp. Primary antibody was incubated overnight for ChIP reactions. Crosslinks were reversed by adding NaCl and heating at 65 °C for 15 h, RNase A was added and incubated for 2 h at 37 °C, and Proteinase K added and incubated 2 h at 63 °C. DNA was isolated using the MinElute PCR Purification Kit (Qiagen 28004). Libraries were made using NEBNext Ultra II Library Kit (E7645) and sequenced on an Illumina Nova Seq at a depth of 100 million paired end reads. Illumina NovaSeq 6000 SRX22322345 GSM7874735_r1 SRP469515 PRJNA1034138 SRS19372956 GSM7874735 GSM7874735 ChIP-Seq GENOMIC ChIP Chromatin was extracted from isolated nuclei and sheared to 100-1000bp. Primary antibody was incubated overnight for ChIP reactions. Crosslinks were reversed by adding NaCl and heating at 65 °C for 15 h, RNase A was added and incubated for 2 h at 37 °C, and Proteinase K added and incubated 2 h at 63 °C. DNA was isolated using the MinElute PCR Purification Kit (Qiagen 28004). Libraries were made using NEBNext Ultra II Library Kit (E7645) and sequenced on an Illumina Nova Seq at a depth of 100 million paired end reads. Illumina NovaSeq 6000 SRX22322346 GSM7874736_r1 SRP469515 PRJNA1034138 SRS19372957 GSM7874736 GSM7874736 ChIP-Seq GENOMIC ChIP Chromatin was extracted from isolated nuclei and sheared to 100-1000bp. Primary antibody was incubated overnight for ChIP reactions. Crosslinks were reversed by adding NaCl and heating at 65 °C for 15 h, RNase A was added and incubated for 2 h at 37 °C, and Proteinase K added and incubated 2 h at 63 °C. DNA was isolated using the MinElute PCR Purification Kit (Qiagen 28004). Libraries were made using NEBNext Ultra II Library Kit (E7645) and sequenced on an Illumina Nova Seq at a depth of 100 million paired end reads. Illumina NovaSeq 6000