chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145341851145341852GA31GENIChomozygous112870784
4145342744145342745TA7GENIChomozygous112870785
4145343247145343248GA21GENICheterozygous112870786
4145345010145345011TC32GENIChomozygous112870788
4145349663145349664GA18GENIChomozygous112870796
4145350121145350122AT19GENIChomozygous112870797
4145350671145350672CT24GENIChomozygous112870798
4145351090145351091CT25GENIChomozygous112870799
4145354146145354147GC19GENIChomozygous112870800
4145354549145354550GA11GENIChomozygous112870801
4145354894145354895CT14GENIChomozygous112870803
4145355614145355615AG13GENIChomozygous112870804
4145356361145356362AC20GENIChomozygous112870805
4145356418145356419TC15GENIChomozygous112870806
4145356424145356425GA12GENIChomozygous112870807
4145356960145356961AT31GENIChomozygous112870808
4145357076145357077TC30GENIChomozygous112870809
4145357179145357180GC14GENIChomozygous112870810
4145357360145357361TA8GENIChomozygous112870811
4145358592145358593CT22GENIChomozygous112870812
4145358857145358858AC22GENIChomozygous126024919
4145358919145358920TC16GENIChomozygous112870813
4145358940145358941AC21GENIChomozygous126024920
4145359534145359535AG31GENIChomozygous112870814
4145359628145359629TG33GENIChomozygous112870815
4145361065145361066AG15GENIChomozygous112870816
4145362996145362997CT30GENIChomozygous112870817
4145364439145364440TC21GENIChomozygous112870819
4145364702145364703CT7GENIChomozygous112870820