chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105889943158899432AG9GENIChomozygous116607436
105890033058900331TA12GENIChomozygous116607442
105890038958900390AG12GENIChomozygous116788062
105890321058903211AG3GENIChomozygous116788064
105890396858903969AG12GENIChomozygous116788066
105890512058905121GA11GENIChomozygous116788068
105890610558906106TC7GENIChomozygous116788070
105890681058906811TG11GENIChomozygous116788072
105891110558911106CT7GENIChomozygous116788074
105891139258911393GA6GENIChomozygous116788076
105891245158912452TC5GENIChomozygous116788078
105891321358913214GA11GENICpossibly homozygous116788080
105891406258914063TC12GENIChomozygous116607456
105891660858916609TC12GENIChomozygous116607460
105891685258916853TC7GENIChomozygous116607462
105891846258918463CG6GENIChomozygous116788082
105891886058918861CA13GENIChomozygous116607466
105891910858919109TC14GENIChomozygous116788084
105892009958920100CT4GENIChomozygous116788086
105892011258920113CT3GENIChomozygous116788088
105892123758921238CT5GENIChomozygous116788090
105892215058922151AC18GENIChomozygous116788092
105892306758923068CT17GENIChomozygous116788094
105892383858923839CA10GENIChomozygous116788096
105892402258924023TG9GENIChomozygous116607476