chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99498371194983712CT30GENICpossibly homozygous52055164
99498422394984224GA37GENIChomozygous53600319
99498435894984359AG41GENIChomozygous52055166
99498489294984893TA36GENIChomozygous52055168
99498493794984938CG35GENIChomozygous53600320
99498510094985101AG35GENIChomozygous52055170
99498528094985281GT27GENICpossibly homozygous52055172
99498530194985302AG28GENIChomozygous52055174
99498533094985331GA32GENICpossibly homozygous52055176
99498537294985373GC25GENICpossibly homozygous52055178
99498538694985387CT25GENICpossibly homozygous52055180
99498603894986039TC27GENIChomozygous52055182
99498694194986942CA22GENIChomozygous52280961
99498736494987365CA22GENIChomozygous53600321
99498952894989529AAT27GENIChomozygous53600322
99498952994989530AT33GENIChomozygous52055198