chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204722545747225458GC19GENIChomozygous109212328
204722551547225516CG17GENIChomozygous109212330
204722557547225576GC9GENIChomozygous109212332
204722627347226274TC38GENIChomozygous109212334
204723586347235864AC29GENIChomozygous109212336
204723586447235865CA29GENIChomozygous109212338
204723964747239648AT42GENIChomozygous109212340
204723966947239670AT45GENIChomozygous109212342
204723967447239675GC46GENIChomozygous109212344
204723968647239687GC51GENIChomozygous109212346
204723970947239710TA46GENIChomozygous109212348
204723974947239750TA43GENIChomozygous109212350
204723975147239752TA44GENIChomozygous109212352
204723985847239859TA43GENIChomozygous109212354
204725375747253758AT47GENICheterozygous109212356
204726075147260752CT77GENICheterozygous109212358
204726078347260784CT82GENICheterozygous109212360
204726079647260797GA76GENICheterozygous109212362
204726273447262735GA46GENICheterozygous109212364
204726277147262772AC85GENICheterozygous109212366
204726281047262811AG135GENICheterozygous109212368
204726283247262833TC139GENICheterozygous109212370
204726286447262865GC138GENICheterozygous109212372
204726287747262878CG138GENICheterozygous109212374
204726288247262883AC139GENICheterozygous109212376
204726288847262889GA136GENICheterozygous109212378
204726302147263022TC149GENICheterozygous109212380
204726309947263100TG167GENICheterozygous109212382