This folder contains compendium of predictions of genetic variants effects summarized per motif
Note: effect column, 1= snp in footprint (no effect on binding) 2 = centisnp (effect on binding)
Genome coordinates are in hg19 (b37)

Columns:
chr
pos    (0-based)
pos1   (1-based)
motif  (motif ID, see factorNames.txt)
footprint_score_lr 
strand  
ref_priorlodds
alt_priorlodds
ref_allele
alt_allele
effect (see note)

The effect of binding is (ref_priorlodds - alt_priorlodds). If positive it means that reference 
allele increases binding. If negative it means that the alternate allele increases binding.
We usually consider absolute score >3 to be a CentiSNP (effect=2), otherwise (effect=1).
3 units of difference in the logOdds scale correspond to 20x fold change in the Odds the SNPs
having an impact on binding.  We can also calculate the posterior log odds of each allele as:

 PostLogOdds_ref = ref_priorlodds + footprint_score_lr
 PostLogOdds_alt = alt_priorlodds + footprint_score_lr