chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118581813585818136CT2GENIChomozygous50854125
118581831885818319TA12GENIChomozygous50854126
118581833885818339GT16GENICpossibly homozygous50854127
118581839585818396GA16GENICpossibly homozygous50854128
118581882485818825CT13GENIChomozygous50854129
118581888385818884AAC16GENIChomozygous50854130
118582056885820569CG17GENICpossibly homozygous50854131
118582141285821413AG23GENIChomozygous50854133
118582149385821494CG14GENIChomozygous50854134
118582166685821667GC8GENICpossibly homozygous50854135
118582249785822498AG19GENIChomozygous50854136
118582378985823790AG15GENICpossibly homozygous50854138
118582388985823890GA17GENIChomozygous50854139
118582404885824049AG19GENIChomozygous50854140
118582407885824079AC18GENICpossibly homozygous50854141