SRX23777712 GSM8117427_r1 SRP492277 PRJNA1081783 SRS20604151 GSM8117427 GSM8117427 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777713 GSM8117428_r1 SRP492277 PRJNA1081783 SRS20602679 GSM8117428 GSM8117428 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777714 GSM8117429_r1 SRP492277 PRJNA1081783 SRS20602678 GSM8117429 GSM8117429 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777715 GSM8117430_r1 SRP492277 PRJNA1081783 SRS20602680 GSM8117430 GSM8117430 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777716 GSM8117431_r1 SRP492277 PRJNA1081783 SRS20603226 GSM8117431 GSM8117431 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777717 GSM8117432_r1 SRP492277 PRJNA1081783 SRS20602681 GSM8117432 GSM8117432 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777718 GSM8117433_r1 SRP492277 PRJNA1081783 SRS20603227 GSM8117433 GSM8117433 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777719 GSM8117434_r1 SRP492277 PRJNA1081783 SRS20602682 GSM8117434 GSM8117434 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777720 GSM8117435_r1 SRP492277 PRJNA1081783 SRS20602683 GSM8117435 GSM8117435 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777721 GSM8117436_r1 SRP492277 PRJNA1081783 SRS20602684 GSM8117436 GSM8117436 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777722 GSM8117437_r1 SRP492277 PRJNA1081783 SRS20604152 GSM8117437 GSM8117437 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777723 GSM8117438_r1 SRP492277 PRJNA1081783 SRS20602686 GSM8117438 GSM8117438 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777724 GSM8117439_r1 SRP492277 PRJNA1081783 SRS20602685 GSM8117439 GSM8117439 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777725 GSM8117440_r1 SRP492277 PRJNA1081783 SRS20602687 GSM8117440 GSM8117440 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777726 GSM8117441_r1 SRP492277 PRJNA1081783 SRS20602688 GSM8117441 GSM8117441 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777727 GSM8117442_r1 SRP492277 PRJNA1081783 SRS20602689 GSM8117442 GSM8117442 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777728 GSM8117443_r1 SRP492277 PRJNA1081783 SRS20602690 GSM8117443 GSM8117443 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000 SRX23777729 GSM8117444_r1 SRP492277 PRJNA1081783 SRS20604456 GSM8117444 GSM8117444 OTHER GENOMIC other Cells were lysed, DNA isolated by phenol/CHCl3/i-amyl alcohol. DNA was sonicated with a Covaris E220 focued ultrasonicator to 200-400 bp size EBndG-DNA was isolated by biotinylation using Click reaaction Libraries were prepared with NEB Ultra IOI Library preparation kit. 3-8 ng DNA was used. Libraries were amplified with 13 cycles on a thermocycle. The libraries were sized selected from 250-450 using Agencourt AMPure XP beads from Beckman. Libraries were validated using the Agilent 2100 Bioanalyzer. Illumina NovaSeq 6000