chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145341858145341859TA36GENIChomozygous119412363
4145342002145342003AG27GENIChomozygous119315385
4145342395145342396AG27GENICpossibly homozygous119412364
4145354146145354147GC19GENIChomozygous112870800
4145354211145354212GA23GENIChomozygous119412365
4145354549145354550GA22GENIChomozygous112870801
4145344921145344922CG9GENICheterozygous119587731
4145354894145354895CT25GENIChomozygous112870803
4145355614145355615AG17GENIChomozygous112870804
4145356361145356362AC25GENIChomozygous112870805
4145356418145356419TC26GENIChomozygous112870806
4145356424145356425GA27GENIChomozygous112870807
4145356960145356961AT28GENIChomozygous112870808
4145357076145357077TC16GENIChomozygous112870809
4145357179145357180GC32GENIChomozygous112870810
4145357360145357361TA21GENIChomozygous112870811
4145358592145358593CT15GENIChomozygous112870812
4145358919145358920TC17GENIChomozygous112870813
4145359534145359535AG19GENIChomozygous112870814
4145359628145359629TG21GENIChomozygous112870815
4145361065145361066AG21GENIChomozygous112870816
4145362996145362997CT17GENIChomozygous112870817
4145363773145363774CT18GENIChomozygous112870818
4145364439145364440TC15GENIChomozygous112870819
4145364702145364703CT21GENIChomozygous112870820