I have a multi-sample vcf file and I want to get a table of IDs on the left column with the variants in which they have an alternate allele in. It should look l
pint
apt
avdepthdata
page-caching
md-autocomplete
bulk-delete
memcpy
two-way-binding
presto-jdbc
sslserversocket
linkbutton
gremlinnet
pyhamcrest
isset
gwt-gin
axis
squish
spam
assembly-reference-path
easymock
maintainability
gearman
kubernetes-metrics
botman
responsestream
http-request
herepy
markdoc
gephi
hotswap