chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143702630143702631AG25GENIChomozygous116100544
7143703495143703496CT23GENIChomozygous116100546
7143703523143703524TC29GENIChomozygous115944575
7143707145143707146GT14GENIChomozygous116100548
7143707516143707517AT15GENIChomozygous115944578
7143708045143708046GA15GENICpossibly homozygous116100550
7143708411143708412CG23GENIChomozygous116100552
7143708860143708861GA31GENIChomozygous116100554
7143708887143708888GA35GENIChomozygous116100556
7143708962143708963AC29GENIChomozygous116100558
7143710452143710453AG9GENIChomozygous115944581
7143710652143710653CT22GENIChomozygous116100560
7143711524143711525CA32GENIChomozygous116100562
7143712172143712173GA17GENIChomozygous116100564
7143712931143712932AG10GENIChomozygous115944586
7143716406143716407GA24GENIChomozygous116100568
7143716724143716725TC27GENIChomozygous115944587
7143716779143716780GA29GENIChomozygous116100569
7143717111143717112AG12GENIChomozygous116100571
7143717427143717428GA23GENIChomozygous116100573
7143717650143717651CT20GENIChomozygous116100575
7143718613143718614GA19GENIChomozygous116100577
7143718725143718726GC22GENIChomozygous115944589
7143719114143719115AG18GENIChomozygous115944590
7143719255143719256GC19GENIChomozygous115944591
7143719607143719608GA41GENICheterozygous116100579
7143719642143719643GT46GENICheterozygous115944592
7143719710143719711GA38GENICheterozygous116100581
7143720021143720022GA27GENIChomozygous116100583
7143720293143720294CG22GENIChomozygous116100585