chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2210881635210881636AG17GENIChomozygous802212730
2210881729210881730GA23GENICpossibly homozygous802212731
2210882761210882762GA27GENIChomozygous802212732
2210883146210883147GA27GENIChomozygous802212733
2210883147210883148CT27GENIChomozygous802212734
2210883210210883211TC31GENIChomozygous802212735
2210883782210883783CT23GENIChomozygous802212736
2210884805210884806GT22GENICpossibly homozygous802212737
2210885012210885013AC35GENIChomozygous802212738
2210886860210886861TC21GENICheterozygous802212739
2210887535210887536CT48GENICheterozygous802212740
2210887998210887999GT18GENIChomozygous802212741
2210889226210889227CT27GENIChomozygous802212742
2210890256210890257GA23GENIChomozygous802212743