chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123245637032456371AG13GENIChomozygous50443638
123245638332456384TTGTGTGTG12GENIChomozygous50933161
123245638432456385AT12GENIChomozygous50933164
123245644232456443GC19GENIChomozygous50443640
123245656132456563GT--6GENICheterozygous50541082
123245675432456755GA22GENIChomozygous50933167
123246034432460345CT8GENIChomozygous50933170
123246049132460492T-15GENIChomozygous50933173
123246064532460646GA18GENIChomozygous50933176
123246067332460674GA19GENIChomozygous50933179
123246114832461149TC16GENIChomozygous50443644
123246147932461495CTTCCTTCCTTCCTTC----------------11GENIChomozygous51017942
123246175132461763CTCTCTCTCTCT------------9GENICheterozygous50933182
123246283732462838TC26GENIChomozygous50443656
123246286732462868CT29GENIChomozygous50443658
123246377932463780TTAC16GENICpossibly homozygous50933185
123246782032467822AC--12GENICheterozygous50541084
123245967732459678C-3GENIChomozygous50175739
123246174932461763CTCTCTCTCTCTCT--------------9GENICheterozygous50968036