chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175079202550792026CT19GENIChomozygous574257803
175079206850792069GC12GENIChomozygous574257804
175079220550792206CG10GENIChomozygous574257805
175079260250792603GA22GENIChomozygous574257806
175079281050792811AG27GENIChomozygous574257807
175079289550792896AG23GENIChomozygous574257808
175079310250793103TTA11GENICheterozygous713483719
175079315150793152AC15GENIChomozygous574257809
175079318450793185AG21GENIChomozygous574257810
175079326350793264T-14GENIChomozygous713483720
175079331450793315TC13GENIChomozygous574257811
175079332850793329CT14GENIChomozygous574257812
175079337850793379CT12GENIChomozygous574257813
175079341450793415AG18GENIChomozygous574257814
175079369550793696CT19GENIChomozygous574257815
175079369650793697GA19GENIChomozygous574257816
175079393650793937AC8GENIChomozygous574257817
175079396450793965AT9GENIChomozygous574257818
175079447650794477CT3GENIChomozygous574257819
175079452150794522GC10GENIChomozygous574257820
175079452850794529GA11GENIChomozygous574257821
175079453750794538CT11GENIChomozygous574257822
175079455650794557GA11GENIChomozygous574257823
175079467750794678TTA3GENIChomozygous713483721
175079467850794679TA3GENIChomozygous574257824
175079505850795059GA24GENIChomozygous574257825
175079520050795201TC12GENIChomozygous574257826
175079567650795677CT19GENIChomozygous574257827
175079672750796728GA15GENIChomozygous574257828
175079678550796786CT9GENIChomozygous574257829
175079713550797136TC18GENIChomozygous574462422
175079759550797596CT16GENIChomozygous574257830
175079812050798121T-21GENIChomozygous713483722
175079827350798274GA37GENIChomozygous574257831
175079842150798422TTGC27GENICpossibly homozygous713483723
175079852150798522CT27GENIChomozygous574257832
175080012550800126AG15GENIChomozygous574257833