chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48841719688417197GT24GENIChomozygous112772559
48841721488417215GA24GENIChomozygous112772560
48841730688417307AT11GENIChomozygous112772561
48841734088417341GC12GENIChomozygous112772562
48841740488417405AG22GENIChomozygous112772563
48841745288417453GA26GENIChomozygous112772564
48841801188418012CT8GENIChomozygous112772565
48841814088418141TC6GENIChomozygous112772566
48841907488419075AG17GENICpossibly homozygous112772567
48841910588419106TC21GENIChomozygous112772568
48841929588419296CT60GENICheterozygous112772569
48841954888419549TC22GENIChomozygous112772570
48841963288419633TC30GENIChomozygous112772571
48842066788420668AC28GENIChomozygous112772572
48842094988420950AG20GENIChomozygous112772573
48842179388421794AG17GENIChomozygous112772574
48842260888422609AC22GENIChomozygous112772575
48842311488423115AG12GENIChomozygous112772576
48842326488423265GT20GENIChomozygous112772577
48842327288423273CT23GENICheterozygous112772578
48842347988423480CT23GENIChomozygous112772579
48842369988423700GC34GENIChomozygous112772580
48842448788424488TA24GENIChomozygous112772581
48842450588424506CG20GENIChomozygous112772582
48842459188424592AG19GENIChomozygous112772583