chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41418139714181398TG3GENIChomozygous56759722
41418140014181401CT3GENIChomozygous56759723
41418361814183619CA1GENIChomozygous56759729
41418370114183702GC11GENIChomozygous56759731
41418375214183753GT2GENIChomozygous56759733
41418394014183941A-3GENICheterozygous56759735
41418396514183966CT4GENICheterozygous56759736
41418434914184350TG5GENIChomozygous56759737
41418494714184948AG9GENICheterozygous56759740
41418496114184962GC11GENICpossibly homozygous56759741
41418504614185047AC5GENICheterozygous56759742
41418582114185822CT16GENICpossibly homozygous56759743
41418708614187087TC11GENICpossibly homozygous56759758
41418583414185835G-20GENICheterozygous58274854
41418585514185859GAAA----18GENICheterozygous58274856
41419347214193473A-4GENIChomozygous56759800
41419548714195488AG5GENICheterozygous56759801
41420379414203795GGA2GENIChomozygous56759805
41421697014216975TTTTT-----5GENICheterozygous58328091