chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5165700013165700014TC29GENIChomozygous71511597
5165700811165700812AT40GENICpossibly homozygous71511601
5165703309165703310AG36GENIChomozygous71511605
5165705216165705217TC23GENIChomozygous71511608
5165707371165707372AG26GENIChomozygous71511612
5165709477165709478TC15GENIChomozygous71511616
5165709487165709488AG16GENIChomozygous71511620