chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133406600133406601TC17GENIChomozygous112832599
4133406762133406763CT20GENIChomozygous112832601
4133406818133406819AG21GENIChomozygous112832602
4133407260133407261AG20GENIChomozygous112832603
4133407364133407365CT24GENICpossibly homozygous113385282
4133407539133407540CT18GENIChomozygous112832604
4133407541133407542CT19GENIChomozygous112832605
4133407651133407652TC18GENIChomozygous112832606
4133408381133408382AG22GENIChomozygous112832607
4133408819133408820TC21GENIChomozygous112832608
4133408859133408860CA22GENIChomozygous112832609
4133410597133410598CT17GENIChomozygous112832612
4133411368133411369GA24GENIChomozygous112832613
4133411563133411564AG20GENIChomozygous113306506
4133411657133411658AG26GENIChomozygous113306507
4133412310133412311CT25GENIChomozygous113306508
4133412869133412870CT16GENIChomozygous113306511
4133412978133412979TG22GENIChomozygous112832617
4133413098133413099GA20GENIChomozygous113306512
4133413540133413541TG26GENIChomozygous119459293