chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141525386715253868G21GENIChomozygous131726603
141525416315254164GA28GENIChomozygous113720061
141525443915254440CT17GENIChomozygous113720063
141525444715254448CT14GENIChomozygous113720065
141525445215254453GA16GENICpossibly homozygous113720067
141525483615254837G24GENIChomozygous129127877
141525493915254940TA21GENIChomozygous113356612
141525574215255743CT24GENIChomozygous113356616
141525576715255768GA21GENIChomozygous113356618
141525578515255786GT22GENIChomozygous113720069
141525593115255932CT27GENIChomozygous113720071
141525599515255996CG29GENIChomozygous113356624
141525610515256106CT26GENIChomozygous113720073
141525684015256841GA27GENIChomozygous113720075
141525722515257226TC26GENIChomozygous113356630
141525724715257248CT27GENIChomozygous113720077
141525739515257396CT20GENIChomozygous113720079
141525761715257617CATCTTGC30GENIChomozygous129127878
141525771615257717CT24GENIChomozygous113720081
141525791415257914A20GENIChomozygous129127879