chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1256786501256786502TC30GENIChomozygous108622720
1256787447256787448CA28GENIChomozygous120512679
1256790225256790226TC29GENIChomozygous108622733
1256790853256790854GC35GENIChomozygous108622736
1256786964256786965TA20GENIChomozygous109024038
1256787659256787660AT35GENIChomozygous109024039
1256788130256788131TC32GENIChomozygous109024040
1256791887256791888GA5GENIChomozygous109024042
1256792080256792081AC22GENIChomozygous109024043
1256792277256792278AG27GENIChomozygous109024044
1256792415256792416CG23GENIChomozygous109024045
1256793007256793008CT20GENIChomozygous108622741
1256793115256793116AG25GENIChomozygous108622742
1256793479256793480CT27GENIChomozygous109024046
1256794754256794755GC19GENIChomozygous109024047
1256795972256795973GA31GENIChomozygous109024048
1256796059256796060GA24GENIChomozygous109024049
1256796285256796286TC40GENIChomozygous109024050
1256796426256796427TC29GENIChomozygous109024051
1256797502256797503GA22GENIChomozygous109024052
1256797907256797908AT9GENIChomozygous109024053
1256798055256798056GA19GENIChomozygous109024054
1256798174256798175GA23GENIChomozygous109024055
1256798525256798526GA33GENIChomozygous108622748
1256799010256799011TC41GENIChomozygous109024056
1256799149256799150TA41GENIChomozygous108622749
1256800344256800345TC27GENIChomozygous109024057
1256800388256800389CT23GENIChomozygous108622752
1256800610256800611TC25GENIChomozygous108622753
1256801088256801089CT22GENIChomozygous108622754
1256801857256801858GA24GENIChomozygous109024058
1256802177256802178CT28GENIChomozygous108622755
1256802206256802207GA29GENIChomozygous108622756
1256802363256802364TG36GENIChomozygous109024059
1256803527256803528GA28GENIChomozygous108622760
1256802604256802605AG35GENIChomozygous108622758