SRX20314403 GSM7336653_r1 SRP437490 PRJNA972007 SRS17638812 GSM7336653 GSM7336653 ChIP-Seq GENOMIC ChIP Cells were fixed with formaldehyde for 10 minutes using the active motif Low cell ChIP-seq (cat # 53084). After quenching and cell lysis, chromatin was sonicated using a Q800R3 Sonicator (Qsonica) with recirculating chiller. ChIP-seq libraries were prepared using the active motif Low cell ChIP-seq (cat # 53084) that include the Next Gen DNA library kit and Next Gen Indexing kit. 10 ng of DNA was used as starting material for input and ip samples. Libraries were amplified using 14 cycles on the thermocycler. Post amplification libraries were size selected at 250-450bp in length using SPRIselect beads from Beckman Coulter. Libraries were validated using the Agilent High Sensitivity DNA Kit. HiSeq X Ten SRX20314404 GSM7336654_r1 SRP437490 PRJNA972007 SRS17638813 GSM7336654 GSM7336654 ChIP-Seq GENOMIC ChIP Cells were fixed with formaldehyde for 10 minutes using the active motif Low cell ChIP-seq (cat # 53084). After quenching and cell lysis, chromatin was sonicated using a Q800R3 Sonicator (Qsonica) with recirculating chiller. ChIP-seq libraries were prepared using the active motif Low cell ChIP-seq (cat # 53084) that include the Next Gen DNA library kit and Next Gen Indexing kit. 10 ng of DNA was used as starting material for input and ip samples. Libraries were amplified using 14 cycles on the thermocycler. Post amplification libraries were size selected at 250-450bp in length using SPRIselect beads from Beckman Coulter. Libraries were validated using the Agilent High Sensitivity DNA Kit. HiSeq X Ten SRX20314405 GSM7336655_r1 SRP437490 PRJNA972007 SRS17638814 GSM7336655 GSM7336655 ChIP-Seq GENOMIC ChIP Cells were fixed with formaldehyde for 10 minutes using the active motif Low cell ChIP-seq (cat # 53084). After quenching and cell lysis, chromatin was sonicated using a Q800R3 Sonicator (Qsonica) with recirculating chiller. ChIP-seq libraries were prepared using the active motif Low cell ChIP-seq (cat # 53084) that include the Next Gen DNA library kit and Next Gen Indexing kit. 10 ng of DNA was used as starting material for input and ip samples. Libraries were amplified using 14 cycles on the thermocycler. Post amplification libraries were size selected at 250-450bp in length using SPRIselect beads from Beckman Coulter. Libraries were validated using the Agilent High Sensitivity DNA Kit. HiSeq X Ten