chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123114207831142079G8GENICheterozygous130407519
123114639031146391A14GENIChomozygous128980752
123114624331146245CG11GENIChomozygous128980748
123114627131146271C11GENIChomozygous128980749
123114633131146332T9GENIChomozygous128980750
123114636031146363CTG11GENIChomozygous128980751
123114642231146422G17GENIChomozygous128980753
123114645231146452C20GENIChomozygous128980754
123114657831146579T9GENIChomozygous128980755
123114662531146626G10GENIChomozygous128980756
123114667331146674T9GENIChomozygous128980757
123114671331146714C15GENIChomozygous128980758
123114672831146728C17GENIChomozygous128980759
123114683131146831T13GENIChomozygous128980760
123114683831146839G13GENIChomozygous128980761
123114685431146855G12GENIChomozygous128980762
123114688431146885G13GENIChomozygous128980763
123114688931146890T13GENIChomozygous128980764
123114690731146908A12GENIChomozygous128980765
123114691231146913G12GENIChomozygous128980766
123114693631146936T9GENIChomozygous128980767
123114698031146981C13GENIChomozygous128980768
123114701231147012C12GENIChomozygous128980769
123114703431147034T9GENIChomozygous128980770
123115216731152167TCCCTTCCTCCTCCTCC9GENIChomozygous128980771
123115217231152172CCT10GENIChomozygous128980772
123115222031152221G13GENIChomozygous128980773