As title.
I am using JASPAR data: MA0058.2(transcription factor: MAX) to scan whole genome(hg19), I found out that JASPAR has already did the job and put the binding site data in the bed_files/ (http://jaspar.binf.ku.dk/html/DOWNLOAD/), there are about 24564 binding sites that it found by using MA0058.2 to scan hg19.
When I use PWMScan (http://ccg.vital-it.ch/pwmscan/) to scan the same data (MA0058.2) in hg19, I got about 131785 binding sites that it found.
I am curious why there is such big range in them?
Which tool is more accuracy or any suggestion tools that I should try?