chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102760840102760841GT29GENIChomozygous61486885
1102761901102761902GA21GENIChomozygous61486886
1102762817102762818AC28GENIChomozygous61486887
1102763041102763042CCA21GENICpossibly homozygous60780097
1102763600102763601TC26GENIChomozygous61486888
1102765800102765801CA21GENIChomozygous61486889