chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
92906847929068480CT11GENICheterozygous51831747
92906870029068701AAT5GENIChomozygous51831749
92906952029069521TC24GENICpossibly homozygous51831755
92906958729069588AG18GENICpossibly homozygous51831757
92907291029072911GA7GENIChomozygous51831767
92907396729073968TC28GENICpossibly homozygous51831769
92907481929074820AG11GENIChomozygous51831771