chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175079202550792026CT23GENIChomozygous47127873
175079206850792069GC26GENIChomozygous47127874
175079220550792206CG23GENIChomozygous47127875
175079260250792603GA21GENIChomozygous47127876
175079281050792811AG22GENIChomozygous47127877
175079289550792896AG31GENIChomozygous47127878
175079310250793103TTA16GENICpossibly homozygous47127879
175079315150793152AC19GENIChomozygous47127880
175079318450793185AG26GENIChomozygous47127881
175079326350793264T-23GENIChomozygous47127882
175079331450793315TC30GENIChomozygous47127883
175079332850793329CT35GENIChomozygous47127884
175079337850793379CT38GENIChomozygous47127885
175079341450793415AG32GENIChomozygous47127886
175079369550793696CT32GENIChomozygous47127887
175079369650793697GA32GENIChomozygous47127888
175079393650793937AC20GENIChomozygous47127889
175079396450793965AT19GENIChomozygous47540942
175079447650794477CT18GENICpossibly homozygous47540944
175079452150794522GC17GENIChomozygous47127890
175079452850794529GA16GENIChomozygous47127891
175079453750794538CT12GENIChomozygous47127892
175079455650794557GA15GENIChomozygous47127893
175079467750794678TTA17GENIChomozygous47127896
175079467850794679TA18GENIChomozygous47127897
175079505850795059GA17GENIChomozygous47127900
175079520050795201TC22GENIChomozygous47127901
175079567650795677CT34GENIChomozygous47127902
175079672750796728GA31GENIChomozygous47127903
175079678550796786CT24GENIChomozygous47127904
175079713550797136TC31GENICpossibly homozygous47127905
175079759550797596CT28GENIChomozygous47127906
175079812050798121T-24GENICpossibly homozygous47540946
175079827350798274GA20GENIChomozygous47540948
175079842150798422TTGC19GENICpossibly homozygous47127907
175079852150798522CT22GENIChomozygous47127911
175080012550800126AG23GENIChomozygous47127912