chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2276130962276130963AAT11GENIChomozygous59588792
2276131801276131802GGACTC19GENIChomozygous59588795
2276133580276133582GG--4GENICheterozygous59588799
2276133817276133818AT17GENIChomozygous59588800
2276136120276136121CT34GENIChomozygous59588803
2276143395276143396CCAA14GENIChomozygous59588814
2276132055276132056AAC25GENIChomozygous60188657
2276132595276132600TATGA-----32GENIChomozygous60188658
2276137094276137102GAGAATTT--------19GENIChomozygous60188659
2276145603276145604CCTTTT9GENICheterozygous60531861
2276138795276138797AT--4GENIChomozygous60996752
2276138811276138823ATATATATATAT------------5GENIChomozygous60996754
2276145603276145604CCT9GENICheterozygous60692287
2276149164276149165A-1GENIChomozygous60996756
2276149836276149837GGCAGACAGACAGACAGACAGACAGACAGA7GENIChomozygous60996758
2276151413276151417CACA----18GENIChomozygous59588828
2276151558276151559TTGAC18GENIChomozygous59588829
2276154332276154333GA27GENIChomozygous60188661
2276156870276156871AG20GENIChomozygous59588832
2276156883276156884TA18GENIChomozygous60188662
2276157633276157634AG22GENIChomozygous59588833
2276157938276157939A-21GENIChomozygous60392448
2276159004276159005TTACACACAC13GENIChomozygous60996760
2276160738276160739C-10GENICpossibly homozygous60996762
2276160740276160757CACACACACACACAAAC-----------------10GENICpossibly homozygous60996764
2276133581276133582G-4GENICheterozygous59986145
2276155305276155310GGTTC-----14GENICheterozygous60564037