It seems like that the primer sequences are highly redundant in the genome or annealing temp is not appropriate at all.

You often see this with this type of PCR. However one usually sees main bands with ghost bands rather than several clear bands. You could increase the annealing temperature but with this i would to be honest make new primers as you could spend a lot of time on this. Another approach is to do a double PCR- take the product of this design primers that are staggered in from this and re-PCR using this as your template.

Hi,

I agree with Prof. Boyd and Dr Shim