chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2276130962276130963AAT10GENIChomozygous59588792
2276131801276131802GGACTC18GENIChomozygous59588795
2276133580276133582GG--7GENICheterozygous59588799
2276133817276133818AT31GENIChomozygous59588800
2276136120276136121CT20GENIChomozygous59588803
2276132055276132056AAC20GENIChomozygous60188657
2276132595276132600TATGA-----25GENIChomozygous60188658
2276133581276133582G-7GENICheterozygous59986145
2276137094276137102GAGAATTT--------16GENIChomozygous60188659
2276143395276143396CCAA4GENIChomozygous59588814
2276151413276151417CACA----21GENIChomozygous59588828
2276151558276151559TTGAC31GENIChomozygous59588829
2276154332276154333GA19GENIChomozygous60188661
2276156870276156871AG18GENIChomozygous59588832
2276156883276156884TA18GENIChomozygous60188662
2276157633276157634AG22GENIChomozygous59588833
2276157938276157939A-17GENIChomozygous60392448
2276160740276160757CACACACACACACAAAC-----------------23GENICpossibly homozygous60996764
2276138795276138797AT--3GENIChomozygous60996752
2276138811276138823ATATATATATAT------------3GENIChomozygous60996754
2276149836276149837GGCAGACAGACAGACAGACAGACAGACAGA9GENIChomozygous60996758
2276159004276159005TTACACACAC11GENIChomozygous60996760
2276160738276160739C-23GENICpossibly homozygous60996762
2276145603276145604CCT2GENICheterozygous60692287