chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175308088053080881CG56GENIChomozygous111062979
175308524253085243TG40GENICpossibly homozygous111062981
175308545653085457AG41GENIChomozygous111062982
175308552153085522GC36GENIChomozygous111062983
175308572253085723GC45GENIChomozygous111062984
175308574753085748CT43GENIChomozygous111062985
175308609953086100AG51GENIChomozygous111062986
175308616253086163AG29GENIChomozygous111062987
175308673253086733TC32GENIChomozygous111062988
175308722953087230GA33GENIChomozygous111062989
175308724453087245TA31GENIChomozygous111062990
175308733253087333TC24GENIChomozygous111062991