chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1162677368162677369CT17GENIChomozygous120508556
1162677429162677430CT9GENIChomozygous108345581
1162678529162678530AG4GENICheterozygous125404124
1162679968162679969CG10GENIChomozygous108345585
1162680019162680020GA15GENIChomozygous120508557
1162680263162680264GC26GENIChomozygous120508558
1162680699162680700GA25GENIChomozygous108345587
1162680958162680959GA12GENIChomozygous108345589
1162682547162682548TG24GENIChomozygous108345595
1162682652162682653CT9GENIChomozygous120508559
1162683381162683382CT20GENIChomozygous108345599
1162684997162684998CG27GENIChomozygous108345605
1162686223162686224AT14GENIChomozygous108345609
1162686528162686529GT6GENIChomozygous108345613
1162687262162687263CT25GENIChomozygous108345617
1162687420162687421CT4GENIChomozygous108345619
1162687707162687708CT8GENIChomozygous125404126
1162688357162688358TG17GENIChomozygous108345621
1162689519162689520GA17GENIChomozygous120508560
1162689551162689552AG5GENIChomozygous120508561
1162689854162689855GT5GENIChomozygous125404128
1162692401162692402GA23GENIChomozygous120508562
1162693183162693184AG19GENIChomozygous108345625
1162693931162693932CT15GENIChomozygous108345627
1162694310162694311GA9GENICheterozygous120508564
1162695747162695748GA22GENIChomozygous120508565
1162696334162696335AT15GENIChomozygous120508566
1162696407162696408GT21GENIChomozygous108345629