chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1162676333162676334AT21GENIChomozygous108345577
1162677227162677228AG12GENIChomozygous108345579
1162677429162677430CT3GENIChomozygous108345581
1162679968162679969CG26GENIChomozygous108345585
1162680699162680700GA29GENIChomozygous108345587
1162682035162682036CT15GENIChomozygous108345591
1162682547162682548TG12GENIChomozygous108345595
1162683276162683277CT17GENIChomozygous108345597
1162683381162683382CT17GENIChomozygous108345599
1162683510162683511GA24GENIChomozygous108345601
1162684997162684998CG20GENIChomozygous108345605
1162685742162685743GT21GENIChomozygous108345607
1162686223162686224AT16GENIChomozygous108345609
1162686427162686428AC7GENIChomozygous108345611
1162686528162686529GT20GENIChomozygous108345613
1162686741162686742GA15GENIChomozygous108345615
1162687262162687263CT22GENIChomozygous108345617
1162687420162687421CT29GENIChomozygous108345619
1162688058162688059AC11GENIChomozygous120474377
1162688357162688358TG20GENIChomozygous108345621
1162689859162689860TG25GENICpossibly homozygous108751148
1162690141162690142GA21GENIChomozygous108345623
1162693183162693184AG16GENIChomozygous108345625
1162693931162693932CT21GENIChomozygous108345627
1162696407162696408GT18GENIChomozygous108345629