Here is the sample output, I bolded the command to distinguish from the data (how I will be using it)...and indicated in blue the data which I would be interested in grabbing for next stage of processing....
[sge@bfdvpc10002m run_2149]$
/opt/pipe/igvtools/igvtools count --strands read --windowSize 1 --query 1:43815031-43815165 B1040_ATCACG_L002.recal.bam stdout /opt/ras/ref/human_GRCh37.68/bwa/genome.faComputing coverage. File = B1040_ATCACG_L002.recal.bam
Max zoom = 7
Window size = 1
Window functions: mean
Ext factor = 0
Loading genome: /opt/ras/ref/human_GRCh37.68/bwa/genome.fa
IGV Directory: /home/sge/igv
Genome loaded. id= /opt/ras/ref/human_GRCh37.68/bwa/genome.fa
track type=wiggle_0
#Columns: Pos, Positive Strand, Negative Strand
variableStep chrom=1 span=1
43815031 23.0 30.0
43815032 23.0 30.0
43815033 24.0 30.0
43815034 24.0 31.0
43815035 24.0 31.0
43815036 24.0 30.0
43815037 24.0 29.0
43815038 23.0 29.0
43815039 22.0 28.0
43815040 21.0 30.0