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
tabitem
parfor
ias
traversal
iso-3166
mobile-config
mtlbuffer
pyiron
mkreversegeocoder
ibm-cloud-speech
embark
paperjs
stubbydb
azure-iot-hub
caffe
workflow-foundation-4
train-test-split
spiffs
nmi
appcmd
fiware
greenlets
completable-future
ejs-schedule
oboe
ewsjavaapi
rollup
parallels
css-validator
organizational-unit