chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153716328337163284AAG18GENICpossibly homozygous48501585
153716501237165013GA11GENICpossibly homozygous48501588
153716715937167160TTG8GENIChomozygous48501596
153716718837167189AT11GENIChomozygous48501598
153716732937167330AG12GENIChomozygous48501600
153716757937167580CT17GENIChomozygous48501602
153716866437168665CG10GENICpossibly homozygous48501604
153716869937168700CT18GENIChomozygous48501606
153716910437169105AG13GENIChomozygous48501608
153716999237169993TC12GENIChomozygous48501610
153717061937170620AG4GENICheterozygous48501612
153717111637171117GA11GENICpossibly homozygous48501614
153717120637171207G-7GENIChomozygous48501616
153717130037171301TC7GENIChomozygous48501618
153717256837172569TC2GENIChomozygous48501622
153717268937172690GA3GENIChomozygous48501626