chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143702630143702631AG6GENIChomozygous116100544
7143703495143703496CT18GENIChomozygous116100546
7143703523143703524TC12GENIChomozygous115944575
7143707516143707517AT19GENIChomozygous115944578
7143708860143708861GA20GENIChomozygous116100554
7143708887143708888GA17GENIChomozygous116100556
7143708962143708963AC24GENIChomozygous116100558
7143710452143710453AG4GENIChomozygous115944581
7143710652143710653CT20GENIChomozygous116100560
7143711524143711525CA18GENIChomozygous116100562
7143712172143712173GA12GENIChomozygous116100564
7143716406143716407GA14GENIChomozygous116100568
7143716724143716725TC11GENIChomozygous115944587
7143716779143716780GA23GENIChomozygous116100569
7143717427143717428GA18GENICpossibly homozygous116100573
7143717650143717651CT21GENIChomozygous116100575
7143718613143718614GA27GENIChomozygous116100577
7143718725143718726GC26GENIChomozygous115944589
7143719255143719256GC11GENIChomozygous115944591
7143720021143720022GA25GENIChomozygous116100583
7143720293143720294CG13GENIChomozygous116100585