chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1169447957169447958TG12GENIChomozygous120488036
1169447960169447961GA11GENIChomozygous109165351
1169449654169449655TG9GENIChomozygous120488037
1169449655169449656AT8GENIChomozygous120488038
1169450967169450968TC18GENIChomozygous108365519
1169451011169451012TA15GENIChomozygous108957456
1169452052169452053AG9GENIChomozygous108365523
1169452612169452613CT12GENIChomozygous108957457
1169452615169452616AT12GENIChomozygous108957458
1169452991169452992CT10GENIChomozygous108957459
1169455697169455698CT14GENIChomozygous108957460
1169456694169456695GA16GENIChomozygous108365530
1169456335169456336TC13GENIChomozygous108365528
1169457674169457675TC15GENIChomozygous108365532
1169457762169457763CT17GENIChomozygous108957461
1169458159169458160AG11GENIChomozygous108365534
1169459677169459678CT7GENIChomozygous108365536
1169459705169459706CT9GENIChomozygous108957462
1169459907169459908GA5GENIChomozygous108957463
1169460661169460662GA12GENIChomozygous108957464
1169460957169460958CT5GENIChomozygous108957465
1169461663169461664AC8GENIChomozygous120488039
1169463428169463429CT13GENICheterozygous108957468