chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18435999284359993CT45GENIChomozygous75426156
18436195184361952CA26GENICpossibly homozygous75426158
18436282284362823CT20GENIChomozygous75426160
18436302284363023GC11GENIChomozygous75426161
18436361584363616GT33GENIChomozygous75426162
18436444784364448TC26GENIChomozygous75426163
18436543784365438GA9GENIChomozygous75426164
18436617284366173TC31GENIChomozygous75426165
18436654884366549TC34GENIChomozygous75426166
18436702284367023CT29GENIChomozygous75426167
18436715784367158AC29GENIChomozygous75046356
18436204784362048AT19GENICheterozygous76632001
18436606984366070AG15GENIChomozygous75684076
18436607084366071GA15GENIChomozygous75684078