chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107248631672486317AG19GENIChomozygous116632673
107248683772486838AG14GENIChomozygous117224038
107248684772486848TC11GENIChomozygous116632677
107248698772486988GA5GENIChomozygous116632679
107248737472487375GT18GENIChomozygous116632683
107248753172487532GT3GENICheterozygous126422989
107248829672488297CT20GENIChomozygous116632685
107248845472488455CT20GENIChomozygous116632687
107248849772488498CT15GENIChomozygous117224040
107248859272488593AC21GENIChomozygous116632689
107248884372488844AG27GENIChomozygous116632691
107248942172489422GA10GENIChomozygous117224042
107248942272489423GA11GENIChomozygous117224044
107248874172488742AG8GENIChomozygous117084575
107248976872489769GA9GENIChomozygous117224048
107249025572490256TC24GENIChomozygous116632693
107249083972490840CT16GENIChomozygous117224050
107249142072491421AC11GENIChomozygous116632697
107249186372491864AG15GENIChomozygous116632699
107249364972493650CT15GENIChomozygous117224052
107249378772493788TC15GENIChomozygous116632705
107249383672493837AG14GENIChomozygous116632707
107249388072493881GA18GENIChomozygous117224054
107249421272494213CT22GENIChomozygous117224056
107249494572494946TA6GENIChomozygous118000963
107249542972495430CT27GENICheterozygous117224058
107249556472495565AG30GENIChomozygous117084612
107249663972496640GA19GENIChomozygous117224060