chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116671425266714253GA38GENIChomozygous973475196
116671647966716480TC30GENIChomozygous973475197
116671668466716685GA26GENIChomozygous973475198
116671730866717309TA7GENICpossibly homozygous973475199
116671760366717604GC18GENIChomozygous973475200
116671771366717714GA15GENIChomozygous973475201
116671894366718944AG21GENIChomozygous973475202
116672098466720985TA17GENIChomozygous973475203
116672232466722325CT17GENIChomozygous973475204
116672350966723510TC29GENIChomozygous973475205
116672411266724113AC16GENIChomozygous973475206
116672422866724229TC19GENIChomozygous973475207
116672543466725435TC13GENIChomozygous973475208
116672636166726362TC26GENIChomozygous973475209
116672675466726755GC37GENIChomozygous973475210
116672734666727347AG28GENIChomozygous973475211
116672886966728870AC19GENICpossibly homozygous973475212
116672908866729089AT22GENIChomozygous973475213
116672959066729591AT25GENIChomozygous973475214
116672969766729698TC13GENIChomozygous973475215
116673084166730842GA33GENIChomozygous973475216