chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62865487028654871CA38GENIChomozygous807661601
62865514228655143CA47GENICpossibly homozygous807661602
62865638228656383GC43GENIChomozygous807661603
62865649928656500TA5GENIChomozygous807661604
62865654928656550TG30GENIChomozygous807661605
62865655028656551TA30GENIChomozygous807661606
62866145328661454AC48GENICpossibly homozygous807661607
62866154028661541AT45GENIChomozygous807661608
62866160128661602GC35GENIChomozygous807661609
62866162928661630GT36GENIChomozygous807661610
62866183328661834TC36GENIChomozygous807661611
62866196328661964AG17GENICpossibly homozygous807661612