chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99336937693369377AT56GENICpossibly homozygous117603462
99337051793370518AG69GENIChomozygous117600561
99337161393371614AG71GENIChomozygous117603470
99337192093371921AG54GENIChomozygous117603472
99337263893372639CT39GENIChomozygous117603478
99337341893373418A48GENIChomozygous132135118
99337342593373426CT57GENIChomozygous117600565
99337479093374793TCT46GENIChomozygous132135119
99337540393375406TTC48GENICpossibly homozygous132135120
99337636593376366C56GENIChomozygous131454017
99337716693377166CCC63GENIChomozygous128732784