chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5149142801149142802CA12GENICpossibly homozygous55787592
5149142877149142878GA20GENIChomozygous55787594
5149142909149142910CT14GENIChomozygous55787596
5149142930149142931GA8GENICpossibly homozygous55787598
5149143079149143080TC25GENIChomozygous55787600
5149143157149143158TC3GENIChomozygous55787602
5149143166149143167T-3GENIChomozygous55787604
5149143182149143183TC3GENIChomozygous55787606
5149143336149143337AG17GENICpossibly homozygous55787608
5149143777149143778GT13GENICpossibly homozygous55787610
5149144056149144057TC20GENICpossibly homozygous55787612
5149144269149144270AAGG5GENIChomozygous55787614
5149144276149144277AG6GENIChomozygous55923748
5149144649149144650GGGT17GENIChomozygous55787616
5149145109149145110AG5GENIChomozygous55787618
5149145126149145127GA4GENICheterozygous55787620
5149145190149145191GA3GENICheterozygous55787622