chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124790436047904361CT46GENIChomozygous930074174
124790442847904429AG26GENIChomozygous930074175
124790503947905040GC42GENIChomozygous930074176
124790533247905333GA13GENIChomozygous930074177
124790592447905925TC44GENIChomozygous930074178
124790718647907187TC19GENIChomozygous930074179
124790723447907235CT30GENIChomozygous930074180
124790755047907551AG51GENIChomozygous930074181
124790807447908075GA32GENIChomozygous930074182
124790818247908183TC55GENIChomozygous930074183
124790853147908532CT35GENIChomozygous930074184
124790978347909784GT37GENIChomozygous930074185
124791088247910883GA52GENIChomozygous930074186
124791103247911033AG45GENIChomozygous930074187
124791118647911187CT43GENIChomozygous930074188
124791211047912111GA30GENIChomozygous930074189
124791214247912143AG32GENIChomozygous930074190
124791233847912339CT50GENIChomozygous930074191
124791237847912379CT38GENIChomozygous930074192
124791252747912528GA38GENIChomozygous930074193
124791252847912529AG38GENIChomozygous930074194
124791329847913299TC44GENIChomozygous930074195
124791396147913962CA36GENIChomozygous930074196
124791396447913965CA36GENIChomozygous930074197
124791409447914095GA48GENIChomozygous930074198
124791421247914213GA22GENIChomozygous930074199
124791539147915392TC60GENIChomozygous930074200
124791703447917035GA35GENICpossibly homozygous930074201
124791720847917209TC51GENIChomozygous930074202
124791936847919369TC55GENIChomozygous930074203
124791985847919859AC42GENIChomozygous930074204