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
fragment-identifier
boost-asio
rayshader
user-defined
quantization
firepath
import-contacts
runit
consul
scrollable
maskededitextender
scheme
qlist
postmessage
targeting
off-screen
fpu
xterm
google-knowledge-graph
undeclared-identifier
zappdev
postal-code
correspondence-analysis
editmode
unnotificationserviceextension
powerpoint
npm-outdated
peephole-optimization
longhorn
google-maps-markers