chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1162676333162676334AT9GENIChomozygous108345577
1162677368162677369CT5GENIChomozygous120508556
1162677429162677430CT12GENIChomozygous108345581
1162679968162679969CG18GENIChomozygous108345585
1162680019162680020GA14GENIChomozygous120508557
1162680263162680264GC19GENIChomozygous120508558
1162680699162680700GA26GENIChomozygous108345587
1162680958162680959GA12GENIChomozygous108345589
1162682547162682548TG17GENIChomozygous108345595
1162682652162682653CT12GENIChomozygous120508559
1162683381162683382CT18GENIChomozygous108345599
1162684997162684998CG28GENIChomozygous108345605
1162686223162686224AT15GENIChomozygous108345609
1162686528162686529GT5GENIChomozygous108345613
1162687262162687263CT17GENIChomozygous108345617
1162687420162687421CT6GENIChomozygous108345619
1162687707162687708CT9GENIChomozygous125404126
1162688357162688358TG27GENIChomozygous108345621
1162689519162689520GA25GENIChomozygous120508560
1162689551162689552AG14GENIChomozygous120508561
1162689854162689855GT5GENICheterozygous125404128
1162692401162692402GA31GENIChomozygous120508562
1162693183162693184AG19GENIChomozygous108345625
1162693931162693932CT13GENIChomozygous108345627
1162694310162694311GA12GENICheterozygous120508564
1162695747162695748GA21GENIChomozygous120508565
1162696334162696335AT23GENIChomozygous120508566
1162696407162696408GT21GENIChomozygous108345629