chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
63495042334950424CCTGTG6GENICheterozygous56073968
63495046334950464AG16GENICheterozygous55493166
63495046734950468GGT19GENICheterozygous55493168
63495046834950469GGTGTGTGTGTGTTT19GENICheterozygous55493170
63495198334951984TTCA22GENICheterozygous54832568
63495263534952636AC18GENIChomozygous54832572
63495292634952927CT25GENIChomozygous54346585
63495292734952928CG25GENIChomozygous54346587
63495293034952931CT26GENIChomozygous54346590
63495293134952932CG26GENIChomozygous54346593
63495294634952947AC30GENIChomozygous54346595
63495295834952959CT24GENIChomozygous54346598
63495298534952987GC--8GENIChomozygous55851210
63495299134952992GA8GENICpossibly homozygous55821055
63495467034954671CT29GENIChomozygous54832582
63495929334959307CACACACACACACA--------------13GENIChomozygous54832626
63496046634960467CCTT3GENICheterozygous55902267
63496210234962103CCTGACTGAA3GENIChomozygous56197248
63496238534962386TG24GENIChomozygous54832664
63496369334963694AT23GENIChomozygous54832676
63496376734963768TC26GENIChomozygous54832680
63496382534963826CCATTTT28GENIChomozygous54832682
63496399434963995AG24GENIChomozygous54832684
63496412134964122CT26GENIChomozygous54832686
63496418134964182GA23GENIChomozygous54865519
63496462834964629GA31GENIChomozygous54865520