chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123961464339614644GA30GENIChomozygous115326335
123961567239615673TC28GENIChomozygous115326337
123961572139615722GA27GENIChomozygous115326339
123961573339615734CT26GENIChomozygous115326341
123961626639616267CT23GENIChomozygous115326343
123961667939616680AG31GENIChomozygous115326345
123961717539617176TC28GENIChomozygous115326347
123961785239617853GT26GENIChomozygous115326349
123961950339619504TC14GENICpossibly homozygous115326351
123961992339619924TC22GENIChomozygous115326353
123962056239620563TC11GENIChomozygous115326355
123962064939620650CT16GENIChomozygous115326357
123962249139622492AG13GENIChomozygous115326359
123962321139623212TG30GENIChomozygous115326361
123962584739625848TC21GENIChomozygous115326363
123962732839627329TC46GENIChomozygous115326365
123963345439633455CT17GENIChomozygous115326371
123963399539633996GA15GENIChomozygous115326373
123963626639636267CT26GENIChomozygous115326375
123963678239636783GC18GENIChomozygous115326377
123963815739638158TA19GENIChomozygous115326379
123963881339638814TC22GENIChomozygous115326381
123963993139639932CT5GENICheterozygous115383349
123964089639640897CT24GENIChomozygous115326383