chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123809583538095836AC28GENICpossibly homozygous813445607
123809689938096900TG7GENICheterozygous813445608
123809695438096955GC15GENIChomozygous813445609
123810097338100974GC36GENIChomozygous813445610
123810111338101114GA16GENIChomozygous813445611
123810112338101124GT13GENIChomozygous813445612
123810317538103176AC39GENIChomozygous813445613
123810334438103345AC21GENIChomozygous813445614
123810441738104418AT20GENIChomozygous813445615
123810489138104892GC26GENIChomozygous813445616
123810613938106140CT15GENICpossibly homozygous813445617
123810640838106409GA22GENIChomozygous813445618
123810672638106727AG25GENIChomozygous813445619
123811057838110579AG29GENIChomozygous813445620
123811099638110997GA27GENIChomozygous813445621
123811392338113924GC10GENIChomozygous813445622
123811394538113946TC8GENIChomozygous813445623
123811451638114517AT27GENIChomozygous813445624
123811644338116444CT23GENICpossibly homozygous813445625