chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31254170112541702TC10GENIChomozygous57154744
31254203812542042AACC----7GENICheterozygous58991944
31254209612542098AC--5GENIChomozygous57154748
31254242212542423C-19GENICpossibly homozygous57154750
31254315412543155AC1GENIChomozygous57154752
31254333712543338TC9GENIChomozygous57154754
31254338012543387GACAGCT-------5GENIChomozygous57154756
31254379812543799CT8GENICpossibly homozygous57154758
31254390112543902TC9GENIChomozygous57154760
31254400012544001GT20GENIChomozygous57154762
31254408212544083CT10GENICpossibly homozygous57154764
31254425012544251CT5GENIChomozygous57154766
31254452712544528CA22GENICpossibly homozygous57154768
31254475112544752GT7GENICheterozygous57154770
31254496912544970TC15GENICpossibly homozygous57154778
31254558712545588TA14GENIChomozygous57154780
31254560412545605AG14GENIChomozygous57154782
31254638312546384CG21GENIChomozygous57154786
31254643212546433CT15GENICpossibly homozygous57154788
31254646312546464GA11GENICheterozygous57154790
31254692112546922AT12GENICpossibly homozygous57154796
31254719312547194TC7GENICpossibly homozygous57154798
31254719412547195GC7GENICpossibly homozygous57154800
31254726612547267TC8GENIChomozygous57154802
31254737712547378CT17GENIChomozygous57154808
31254766812547669AAG11GENIChomozygous57154810
31254776912547770CT9GENICpossibly homozygous57154812
31254780712547808CT17GENIChomozygous57154814
31254829012548291GA18GENIChomozygous57154816
31254849512548496AG7GENIChomozygous57154818
31254850312548504TC4GENIChomozygous57154820
31254866512548666AC18GENICpossibly homozygous57154822
31254897212548973GT16GENIChomozygous57154824
31254996712549968GA19GENICpossibly homozygous57154826
31255018312550184TC4GENIChomozygous59826197
31255021212550213TG4GENIChomozygous57154828
31255121612551217GA31GENICheterozygous57154831
31255228912552290A-7GENIChomozygous57154833
31255262012552621TC10GENIChomozygous57154835