chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1256787843256787844TG19GENICpossibly homozygous882115663
1256790225256790226TC6GENIChomozygous882115664
1256790589256790590AT17GENIChomozygous882115665
1256790667256790668GA18GENIChomozygous882115666
1256791059256791060CT30GENIChomozygous882115667
1256792775256792776CT15GENIChomozygous882115668
1256792943256792944CT22GENIChomozygous882115669
1256793007256793008CT26GENIChomozygous882115670
1256793047256793048CT13GENIChomozygous882115671
1256793115256793116AG20GENIChomozygous882115672
1256793973256793974CA20GENIChomozygous882115673
1256796059256796060GA31GENIChomozygous882115674
1256796285256796286TC21GENIChomozygous882115675
1256796426256796427TC20GENIChomozygous882115676
1256797502256797503GA26GENIChomozygous882115677
1256797907256797908AT9GENIChomozygous882115678
1256798055256798056GA14GENIChomozygous882115679
1256798174256798175GA21GENIChomozygous882115680
1256798389256798390AG20GENIChomozygous882115681
1256798525256798526GA21GENIChomozygous882115682
1256799010256799011TC8GENICheterozygous882115683
1256800196256800197AG21GENIChomozygous882115684
1256800344256800345TC13GENIChomozygous882115685
1256800388256800389CT10GENICheterozygous882115686
1256800610256800611TC29GENIChomozygous882115687
1256801088256801089CT7GENIChomozygous882115688
1256801616256801617GA3GENICheterozygous882115689
1256801644256801645GC11GENIChomozygous882115690
1256801756256801757AT4GENIChomozygous882115691
1256801857256801858GC14GENIChomozygous882115692
1256802177256802178CT22GENIChomozygous882115693
1256802206256802207GA30GENIChomozygous882115694