Support for fitCons: indicator of potential for interesting function in genomic variants

fitCons supplements existing scores in GEMINI like CADD and dbNSFP for
identifying variants with potential for functional impact. It
specifically aims to improve this identification in non-coding regions:

http://haldanessieve.org/2014/09/12/our-paper-probabilities-of-fitness-consequences-for-point-mutations-across-the-human-genome/