chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5138246469138246470CT49GENIChomozygous114027150
5138248084138248085GT64GENIChomozygous114027152
5138248141138248142CT60GENIChomozygous114027154
5138248545138248546GA64GENIChomozygous114027156
5138248703138248704GC45GENIChomozygous114027158
5138249488138249489AG45GENICpossibly homozygous114027160
5138249817138249818TA59GENIChomozygous114027161
5138249845138249846CT54GENIChomozygous114027162
5138250163138250164AC44GENIChomozygous114027163
5138250460138250461CT50GENIChomozygous114027164
5138250669138250670GA44GENIChomozygous114027165
5138250691138250692AG50GENIChomozygous114027166
5138251039138251039CAGT53GENIChomozygous128244926
5138246771138246772C52GENIChomozygous128244923
5138247933138247933A47GENIChomozygous128244924
5138250131138250131C44GENIChomozygous128244925