SRX15036224 GSM6070230_r1 SRP372587 PRJNA832806 SRS12782992 GSM6070230 GSM6070230 ChIP-Seq GENOMIC ChIP Cells were fixed with 1% formaldehyde for 10 minutes. Samples were Mnase treated for 6 minutes and sonicated to achieve desired chromatin banding of 150-900bp. IP was performed overnight with clone D5E4 for H3k27ac using the magnetic SimpleChIP kit (Cell Signaling) Indexed libraries were generated using the ThruPLEX DNA-seq kit (Takara; Mountain View, CA) with 13 cycles of amplification ChIPseq. 1 x 50 bp sequencing was performed on a NovaSeq 6000 (Illumina; San Diego, CA). Illumina NovaSeq 6000 SRX15036225 GSM6070231_r1 SRP372587 PRJNA832806 SRS12782993 GSM6070231 GSM6070231 ChIP-Seq GENOMIC ChIP Cells were fixed with 1% formaldehyde for 10 minutes. Samples were Mnase treated for 6 minutes and sonicated to achieve desired chromatin banding of 150-900bp. IP was performed overnight with clone D5E4 for H3k27ac using the magnetic SimpleChIP kit (Cell Signaling) Indexed libraries were generated using the ThruPLEX DNA-seq kit (Takara; Mountain View, CA) with 13 cycles of amplification ChIPseq. 1 x 50 bp sequencing was performed on a NovaSeq 6000 (Illumina; San Diego, CA). Illumina NovaSeq 6000 SRX15036226 GSM6070232_r1 SRP372587 PRJNA832806 SRS12782994 GSM6070232 GSM6070232 ChIP-Seq GENOMIC ChIP Cells were fixed with 1% formaldehyde for 10 minutes. Samples were Mnase treated for 6 minutes and sonicated to achieve desired chromatin banding of 150-900bp. IP was performed overnight with clone D5E4 for H3k27ac using the magnetic SimpleChIP kit (Cell Signaling) Indexed libraries were generated using the ThruPLEX DNA-seq kit (Takara; Mountain View, CA) with 13 cycles of amplification ChIPseq. 1 x 50 bp sequencing was performed on a NovaSeq 6000 (Illumina; San Diego, CA). Illumina NovaSeq 6000 SRX15036227 GSM6070233_r1 SRP372587 PRJNA832806 SRS12782995 GSM6070233 GSM6070233 ChIP-Seq GENOMIC ChIP Cells were fixed with 1% formaldehyde for 10 minutes. Samples were Mnase treated for 6 minutes and sonicated to achieve desired chromatin banding of 150-900bp. IP was performed overnight with clone D5E4 for H3k27ac using the magnetic SimpleChIP kit (Cell Signaling) Indexed libraries were generated using the ThruPLEX DNA-seq kit (Takara; Mountain View, CA) with 13 cycles of amplification ChIPseq. 1 x 50 bp sequencing was performed on a NovaSeq 6000 (Illumina; San Diego, CA). Illumina NovaSeq 6000 SRX15036228 GSM6070234_r1 SRP372587 PRJNA832806 SRS12783230 GSM6070234 GSM6070234 ChIP-Seq GENOMIC ChIP Cells were fixed with 1% formaldehyde for 10 minutes. Samples were Mnase treated for 6 minutes and sonicated to achieve desired chromatin banding of 150-900bp. IP was performed overnight with clone D5E4 for H3k27ac using the magnetic SimpleChIP kit (Cell Signaling) Indexed libraries were generated using the ThruPLEX DNA-seq kit (Takara; Mountain View, CA) with 13 cycles of amplification ChIPseq. 1 x 50 bp sequencing was performed on a NovaSeq 6000 (Illumina; San Diego, CA). Illumina NovaSeq 6000 SRX15036229 GSM6070235_r1 SRP372587 PRJNA832806 SRS12782996 GSM6070235 GSM6070235 ChIP-Seq GENOMIC ChIP Cells were fixed with 1% formaldehyde for 10 minutes. Samples were Mnase treated for 6 minutes and sonicated to achieve desired chromatin banding of 150-900bp. IP was performed overnight with clone D5E4 for H3k27ac using the magnetic SimpleChIP kit (Cell Signaling) Indexed libraries were generated using the ThruPLEX DNA-seq kit (Takara; Mountain View, CA) with 13 cycles of amplification ChIPseq. 1 x 50 bp sequencing was performed on a NovaSeq 6000 (Illumina; San Diego, CA). Illumina NovaSeq 6000 SRX15036230 GSM6070236_r1 SRP372587 PRJNA832806 SRS12783342 GSM6070236 GSM6070236 ChIP-Seq GENOMIC ChIP Cells were fixed with 1% formaldehyde for 10 minutes. Samples were Mnase treated for 6 minutes and sonicated to achieve desired chromatin banding of 150-900bp. IP was performed overnight with clone D5E4 for H3k27ac using the magnetic SimpleChIP kit (Cell Signaling) Indexed libraries were generated using the ThruPLEX DNA-seq kit (Takara; Mountain View, CA) with 13 cycles of amplification ChIPseq. 1 x 50 bp sequencing was performed on a NovaSeq 6000 (Illumina; San Diego, CA). Illumina NovaSeq 6000 SRX15036231 GSM6070237_r1 SRP372587 PRJNA832806 SRS12782997 GSM6070237 GSM6070237 ChIP-Seq GENOMIC ChIP Cells were fixed with 1% formaldehyde for 10 minutes. Samples were Mnase treated for 6 minutes and sonicated to achieve desired chromatin banding of 150-900bp. IP was performed overnight with clone D5E4 for H3k27ac using the magnetic SimpleChIP kit (Cell Signaling) Indexed libraries were generated using the ThruPLEX DNA-seq kit (Takara; Mountain View, CA) with 13 cycles of amplification ChIPseq. 1 x 50 bp sequencing was performed on a NovaSeq 6000 (Illumina; San Diego, CA). Illumina NovaSeq 6000 SRX15036232 GSM6070238_r1 SRP372587 PRJNA832806 SRS12782998 GSM6070238 GSM6070238 ChIP-Seq GENOMIC ChIP Cells were fixed with 1% formaldehyde for 10 minutes. Samples were Mnase treated for 6 minutes and sonicated to achieve desired chromatin banding of 150-900bp. IP was performed overnight with clone D5E4 for H3k27ac using the magnetic SimpleChIP kit (Cell Signaling) Indexed libraries were generated using the ThruPLEX DNA-seq kit (Takara; Mountain View, CA) with 13 cycles of amplification ChIPseq. 1 x 50 bp sequencing was performed on a NovaSeq 6000 (Illumina; San Diego, CA). Illumina NovaSeq 6000 SRX15036233 GSM6070239_r1 SRP372587 PRJNA832806 SRS12782999 GSM6070239 GSM6070239 ChIP-Seq GENOMIC ChIP Cells were fixed with 1% formaldehyde for 10 minutes. Samples were Mnase treated for 6 minutes and sonicated to achieve desired chromatin banding of 150-900bp. IP was performed overnight with clone D5E4 for H3k27ac using the magnetic SimpleChIP kit (Cell Signaling) Indexed libraries were generated using the ThruPLEX DNA-seq kit (Takara; Mountain View, CA) with 13 cycles of amplification ChIPseq. 1 x 50 bp sequencing was performed on a NovaSeq 6000 (Illumina; San Diego, CA). Illumina NovaSeq 6000 SRX15036234 GSM6070240_r1 SRP372587 PRJNA832806 SRS12783343 GSM6070240 GSM6070240 ChIP-Seq GENOMIC ChIP Cells were fixed with 1% formaldehyde for 10 minutes. Samples were Mnase treated for 6 minutes and sonicated to achieve desired chromatin banding of 150-900bp. IP was performed overnight with clone D5E4 for H3k27ac using the magnetic SimpleChIP kit (Cell Signaling) Indexed libraries were generated using the ThruPLEX DNA-seq kit (Takara; Mountain View, CA) with 13 cycles of amplification ChIPseq. 1 x 50 bp sequencing was performed on a NovaSeq 6000 (Illumina; San Diego, CA). Illumina NovaSeq 6000 SRX15036235 GSM6070241_r1 SRP372587 PRJNA832806 SRS12783196 GSM6070241 GSM6070241 ChIP-Seq GENOMIC ChIP Cells were fixed with 1% formaldehyde for 10 minutes. Samples were Mnase treated for 6 minutes and sonicated to achieve desired chromatin banding of 150-900bp. IP was performed overnight with clone D5E4 for H3k27ac using the magnetic SimpleChIP kit (Cell Signaling) Indexed libraries were generated using the ThruPLEX DNA-seq kit (Takara; Mountain View, CA) with 13 cycles of amplification ChIPseq. 1 x 50 bp sequencing was performed on a NovaSeq 6000 (Illumina; San Diego, CA). Illumina NovaSeq 6000