chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2226855227226855228AC29GENIChomozygous60083292
2226855237226855238CCA28GENIChomozygous60083293
2226855276226855277CT30GENIChomozygous60083294
2226855851226855852AG31GENIChomozygous59421517
2226855945226855946TC21GENIChomozygous60083295
2226856200226856201CT28GENIChomozygous60083296
2226857181226857183TA--13GENIChomozygous60083297
2226857815226857816TC29GENIChomozygous60083298
2226857966226857967GC42GENIChomozygous60083299
2226858271226858272AG25GENIChomozygous60083300
2226858949226858953GCGT----11GENICpossibly homozygous60083301
2226860588226860589AG58GENICheterozygous60083302
2226860875226860876TC35GENIChomozygous60083303
2226861668226861669TTGCACAC37GENIChomozygous60083304
2226861674226861675GC47GENICheterozygous60083305
2226861676226861678TA--44GENICheterozygous60083306
2226862064226862065CCA17GENICpossibly homozygous60083307
2226862180226862181CT27GENIChomozygous60083308
2226862510226862511CT40GENIChomozygous60083309
2226863715226863716TC34GENIChomozygous60083310
2226863820226863821CT35GENIChomozygous60083311
2226864886226864887T-33GENIChomozygous60083312
2226865356226865357AT27GENIChomozygous60083313
2226868234226868235G-13GENIChomozygous60083314
2226868248226868249GGT17GENIChomozygous59421521