chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96576390465763905GC19GENIChomozygous117710290
96577028865770289CT28GENIChomozygous117710294
96577014165770142TC47GENIChomozygous117580072
96577143265771433CA25GENIChomozygous117710296
96577153765771538AG31GENIChomozygous117710298
96577194465771945TG33GENIChomozygous117710300
96577201765772018TG27GENIChomozygous117710302
96577205265772053AG31GENICpossibly homozygous117710304
96577331165773312GA35GENIChomozygous117710306
96577462565774626TC30GENIChomozygous117710308
96577516365775164AG23GENIChomozygous117367451
96577545865775459CT33GENIChomozygous117710310
96577596865775969GA39GENIChomozygous117710312
96577608265776083AG33GENIChomozygous117710314
96577670265776703GT24GENIChomozygous117710316
96577764665777647GC33GENIChomozygous117710318
96577895365778954AG24GENIChomozygous117710320
96577914365779144GT33GENIChomozygous117710322
96578069565780696TC33GENIChomozygous117710324
96578170265781703CT27GENIChomozygous117710328
96578184565781846TC19GENIChomozygous117710330