Reads are mapped to hg38.
Open in IGV and "group by" tag CC.

Tag information:
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BC = sample barcodes for mixing libraries
CC = chromosome cluster index (unique for each cluster in chromosome)
PC = positions covered by cluster
SC = sample code for two seperate libraries: either A1 or B2
DF = "degenerate flag" set to 1 if there is a second mapping [of the four conversion genome mappings] that is equally good
RG = read group indicates sequencing run and sample barcode group
CI = cluster index for local partition
PI = partition index
TI = tag index for both read1 and read2 as: (read1 reverse complemented):(read1 sample tag):(read1 varietal tag):(read2 reverse complemented):(read2 sample tag):(read2 varietal tag)
CM = CC modulo 100
LO = initial left (mapping 3' ref) varietal tag
RO = initial right (mapping 5' ref) varietal tag
LT = error-corrected left varietal tag
RT = error-corrected left varietal tag
IT = invalid tags (misoriented with respect to mapping)
OT = matches reference top strand (0 = reference bottom strand; 1 = reference top strand)
WT = concatentation of well-tags
LW = left well tag
RW = right well tag