chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108213131982131320G-11GENIChomozygous51516668
108213134682131347C-16GENIChomozygous51516669
108213362682133627A-11GENIChomozygous53530158
108213897882138979GT7GENIChomozygous51516720
108213898382138984CT8GENIChomozygous51516721
108213899882138999GT8GENIChomozygous51516722
108213900082139001AT8GENIChomozygous51516723
108213900782139008AT9GENIChomozygous51516724
108213901982139020AT12GENIChomozygous51516725
108213925882139259CG11GENIChomozygous51516729
108213926282139263AAG10GENIChomozygous51516730
108213926882139269A-10GENIChomozygous51516731
108215503282155033T-11GENICheterozygous51516783
108215976882159772ATTT----7GENIChomozygous51717191
108216145982161460GA24INTERGENICheterozygous51516799
108216167882161679T-25INTERGENICheterozygous52390730
108216167882161679TC25INTERGENICheterozygous53530159
108216168182161682TC28INTERGENICheterozygous53530160
108216193082161931TC18INTERGENICheterozygous53530161
108218064082180641T-11GENICheterozygous51717237
108218548182185482CCA11GENIChomozygous51516834