chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143702630143702631AG60GENIChomozygous116100544
7143702638143702638AAC62GENIChomozygous131026071
7143703150143703167TAAATAAATAAATAAAT82GENIChomozygous131026072
7143703495143703496CT53GENIChomozygous116100546
7143707870143707871G46GENICheterozygous128531479
7143707145143707146GT73GENIChomozygous116100548
7143706514143706515G45GENIChomozygous128531478
7143703523143703524TC59GENIChomozygous115944575
7143707516143707517AT59GENIChomozygous115944578
7143708045143708046GA62GENIChomozygous116100550
7143708860143708861GA58GENIChomozygous116100554
7143708887143708888GA60GENIChomozygous116100556
7143708962143708963AC60GENIChomozygous116100558
7143709754143709755T58GENIChomozygous131026073
7143710452143710453AG57GENIChomozygous115944581
7143710652143710653CT62GENIChomozygous116100560
7143711524143711525CA65GENIChomozygous116100562
7143712172143712173GA50GENICpossibly homozygous116100564
7143712931143712932AG42GENIChomozygous115944586
7143712982143712983TC45GENIChomozygous116100566
7143713307143713308A35GENIChomozygous131026074
7143716406143716407GA54GENIChomozygous116100568
7143716565143716565TA56GENIChomozygous128531480
7143716724143716725TC62GENIChomozygous115944587
7143716779143716780GA63GENIChomozygous116100569
7143717111143717112AG71GENIChomozygous116100571
7143717427143717428GA68GENIChomozygous116100573
7143717650143717651CT60GENIChomozygous116100575
7143718613143718614GA47GENIChomozygous116100577
7143718725143718726GC59GENIChomozygous115944589
7143719114143719115AG40GENIChomozygous115944590
7143719255143719256GC33GENIChomozygous115944591
7143719607143719608GA19GENICpossibly homozygous116100579
7143719710143719711GA25GENIChomozygous116100581
7143720021143720022GA40GENIChomozygous116100583
7143720293143720294CG51GENIChomozygous116100585