Yum, beautiful regulatory variants to spot...

Regul@tionSpotter - annotation of extranscriptic variants

   
chromosome     position
reference allele alternative allele
     
   
variant in HGVS notation (currently only possible for SNVs) e.g. chr15:38852120A>T
 
For InDels, use the VCF format, i.e. always start with the last reference base before the variant.
Current build: GRCh 37 / Ensembl 84