chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103625020436250205GA29GENIChomozygous142232516
103625156236251563AG22GENIChomozygous142232517
103625188436251885GA21GENIChomozygous142232518
103625382236253823AT26GENIChomozygous138766365
103625408936254090GT34GENIChomozygous144866155
103625413536254136TC29GENIChomozygous142232519
103625820836258209TG37GENIChomozygous142232520
103626137636261377CT27GENIChomozygous142232521
103626175136261752AC19GENICpossibly homozygous142232522