ad bioinformatics subgroup: I think we should start as a virtual group first. I would be very interested to join and contribute !
In our NIH CC repository, we have 800+ exome data in VCF format (and 1000 more comming in 2015) (as files in BLOB and also as rows in a designated variation table) and a genomic BI report (in Cognos) where you can combine phenotype with genomic data.
(see the report in a video here (jump to time 9min and 30sec)
http://videocast.nih.gov/summary.asp?Live=15002&bhcp=1