chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144448060944480609CC16GENIChomozygous134445340
144448074344480743C15GENICheterozygous134445341
144448086044480861GA42GENIChomozygous125981853
144448239344482394GA61GENIChomozygous125981855
144448452044484522CA2GENIChomozygous129152883
144448454644484546T6GENIChomozygous129152885
144448360044483601A33GENIChomozygous129152882
144448452844484530GG3GENIChomozygous129152884
144448455244484553C7GENIChomozygous129152886
144448455844484559C8GENIChomozygous129152887
144448458344484584C12GENIChomozygous129152888
144448460744484608C16GENIChomozygous129152889
144448463844484639C21GENIChomozygous129152890
144448465844484658G24GENIChomozygous129152891
144448466644484668GC24GENIChomozygous129152892
144448467244484673C24GENIChomozygous129152893
144448467444484675C24GENIChomozygous129152894
144448471644484717C26GENIChomozygous129152895
144448471944484719G27GENIChomozygous129152896
144448473344484734A29GENIChomozygous129152897
144448474544484745T27GENIChomozygous129152898
144448541944485419T8GENIChomozygous134445342
144448582844485836CACCACAC36GENIChomozygous134445343
144448618344486183TTTG43GENIChomozygous132724711
144449303744493037T45GENICheterozygous134445344
144449738444497385CA38GENIChomozygous125981858
144449786444497864G13GENIChomozygous134445345
144449938244499383GA58GENIChomozygous125981860
144450195644501957GC45GENIChomozygous125981862
144448456744484568TG9GENIChomozygous113676807
144448456944484570CT9GENIChomozygous113676809
144448564944485650A32GENICpossibly homozygous130140165
144448922444489225CT28GENIChomozygous134450240
144448929144489292TG24GENIChomozygous113995303
144449325744493258CA32GENIChomozygous118831028