chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83671811836718119CT20GENICpossibly homozygous645346917
83671859236718593GT23GENIChomozygous645346918
83671895136718952AG24GENIChomozygous645346919
83671895236718953AC24GENIChomozygous645346920
83671915436719155GA26GENIChomozygous645346921
83671970036719701AAGT18GENIChomozygous754276055
83671971536719716GA16GENIChomozygous645346922
83672007136720073GC--13GENIChomozygous754276056
83672008036720086CACACA------14GENICheterozygous754276057
83672008236720086CACA----14GENICpossibly homozygous754276058
83672128136721282TC26GENIChomozygous645346923
83672187436721875AG25GENIChomozygous645346924