chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5137772977137772978AG9GENIChomozygous55745624
5137779616137779630CACACAAGCACACA--------------1GENIChomozygous56354902
5137779677137779679AC--2GENIChomozygous55745636
5137779703137779704GGCACA2GENICheterozygous56563243
5137780825137780826TC9GENIChomozygous55745638
5137781501137781502TC17GENIChomozygous55745639
5137782058137782059TC19GENIChomozygous55745640
5137783536137783537GT2GENIChomozygous55745641
5137783853137783854AC4GENIChomozygous55745643
5137785755137785756TC6GENICheterozygous55745646
5137785846137785847TC4GENICheterozygous56233330
5137785847137785848CT4GENICheterozygous56354903
5137786438137786439G-2GENIChomozygous55745647
5137786791137786792AG2GENIChomozygous55745649
5137786897137786898TC13GENICpossibly homozygous55745650
5137787447137787448GC2GENIChomozygous55745651
5137787661137787662CT8GENIChomozygous55745652
5137788482137788483GA1GENIChomozygous55745654
5137790363137790364GT3GENIChomozygous55745655
5137790482137790483CT6GENIChomozygous55745659
5137793156137793157AG7GENIChomozygous55745662
5137793905137793906CG16GENIChomozygous55745663
5137794943137794944TTCC2GENICheterozygous55745666
5137795958137795959CT11GENIChomozygous55745667
5137796002137796003T-6GENIChomozygous55745668
5137796780137796781TC14GENICpossibly homozygous55745669
5137797642137797643GA13GENIChomozygous55745670
5137798719137798720AG16GENIChomozygous55745671
5137798784137798785TA10GENIChomozygous55745672
5137798789137798790GA14GENIChomozygous55745673
5137799060137799061AG14GENIChomozygous55745674
5137799077137799078GC17GENICpossibly homozygous55745675
5137799121137799122GA14GENICpossibly homozygous55745676