chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2276130962276130963AAT6GENICheterozygous59588792
2276131801276131802GGACTC8GENICheterozygous59588795
2276133817276133818AT18GENICheterozygous59588800
2276136120276136121CT14GENICpossibly homozygous59588803
2276132055276132056AAC9GENIChomozygous60188657
2276132595276132600TATGA-----10GENIChomozygous60188658
2276137094276137102GAGAATTT--------2GENIChomozygous60188659
2276133581276133582G-4GENICheterozygous59986145
2276142533276142534A-8GENICheterozygous59781819
2276143395276143396CCAA5GENICheterozygous59588814
2276143395276143396CCA5GENICheterozygous59588815
2276151413276151417CACA----2GENIChomozygous59588828
2276151558276151559TTGAC7GENIChomozygous59588829
2276154332276154333GA14GENICheterozygous60188661
2276156870276156871AG6GENICheterozygous59588832
2276156883276156884TA4GENIChomozygous60188662
2276157633276157634AG20GENIChomozygous59588833