chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106377610663776107GC30GENIChomozygous813177523
106377622363776224AG20GENIChomozygous813177524
106377740763777408AG20GENIChomozygous813177525
106377820363778204CA20GENIChomozygous813177526
106377983363779834GT11GENIChomozygous813177527
106377986863779869AC12GENIChomozygous813177528
106378004863780049GT20GENIChomozygous813177529
106378039763780398AC17GENIChomozygous813177530
106378056363780564GT13GENIChomozygous813177531
106378074563780746AT12GENIChomozygous813177532
106378078263780783CT9GENIChomozygous813177533
106378104263781043CG16GENIChomozygous813177534
106378119563781196CG8GENIChomozygous813177535
106378120663781207GT21GENIChomozygous813177536
106378136063781361AC10GENIChomozygous813177537
106378148363781484GT19GENIChomozygous813177538
106378207463782075TC21GENIChomozygous813177539
106378294663782947CT33GENIChomozygous813177540
106378473463784735AT54GENIChomozygous813177541
106378485563784856GA50GENIChomozygous813177542
106378634463786345CT30GENIChomozygous813177543
106378802363788024CT17GENICpossibly homozygous813177544
106378870963788710GC38GENICheterozygous813177545
106378928963789290TC24GENIChomozygous813177546
106378943963789440GT31GENIChomozygous813177547
106379062063790621AC36GENIChomozygous813177548
106379067163790672TC38GENIChomozygous813177549
106379087663790877AG17GENIChomozygous813177550
106379279163792792GA55GENIChomozygous813177551
106379419263794193CT15GENIChomozygous813177552
106379419663794197CT13GENIChomozygous813177553
106379421263794213TC10GENICheterozygous813177554
106379449263794493AC18GENIChomozygous813177555
106379451963794520GC14GENIChomozygous813177556
106379453263794533GC19GENIChomozygous813177557
106379466163794662GT34GENIChomozygous813177558
106379474163794742GC30GENIChomozygous813177559
106379501463795015TC26GENIChomozygous813177560