chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1169447957169447958TG21GENIChomozygous120488036
1169447960169447961GA20GENIChomozygous109165351
1169449654169449655TG20GENIChomozygous120488037
1169449655169449656AT20GENIChomozygous120488038
1169450967169450968TC28GENIChomozygous108365519
1169451011169451012TA25GENIChomozygous108957456
1169452052169452053AG22GENIChomozygous108365523
1169452612169452613CT22GENIChomozygous108957457
1169452615169452616AT22GENIChomozygous108957458
1169452991169452992CT23GENIChomozygous108957459
1169455697169455698CT27GENIChomozygous108957460
1169456335169456336TC38GENIChomozygous108365528
1169456694169456695GA21GENIChomozygous108365530
1169457674169457675TC35GENIChomozygous108365532
1169457762169457763CT24GENIChomozygous108957461
1169458159169458160AG35GENIChomozygous108365534
1169459677169459678CT19GENIChomozygous108365536
1169459705169459706CT23GENIChomozygous108957462
1169459907169459908GA12GENIChomozygous108957463
1169460661169460662GA23GENIChomozygous108957464
1169460957169460958CT20GENIChomozygous108957465
1169461032169461033GC22GENIChomozygous108957466
1169461648169461649AT6GENIChomozygous120811416
1169461663169461664AC6GENIChomozygous120488039
1169463428169463429CT12GENIChomozygous108957468