chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2038294133829413GGC13GENIChomozygous131227112
2038299673829968TC9GENIChomozygous109070093
2038300013830002TC9GENIChomozygous109070095
2038303393830340TC11GENIChomozygous109070099
2038306153830616AG20GENIChomozygous109070101
2038310373831038CT14GENIChomozygous109070103
2038320853832086AG16GENIChomozygous109070105
2038324283832429CT10GENIChomozygous109070107
2038331883833189TC12GENIChomozygous109070109
2038384453838446TC20GENIChomozygous119756726
2038400563840057GA13GENIChomozygous109070111
2038402793840280CT17GENIChomozygous119756727
2038331073833108GT16GENICpossibly homozygous109417533
2038323553832359TCTT13GENIChomozygous129651558
2038337073833708GA2GENIChomozygous129706073
2038379513837952AG4GENIChomozygous129706076
2038392973839298TG5GENIChomozygous129706077
2038405533840554GA8GENIChomozygous129706078
2038491733849174TG13GENIChomozygous109541872
2038493143849315CT21GENIChomozygous119867686
2038493953849396CT18GENIChomozygous109070113
2038494903849490G9GENIChomozygous129651560
2038497663849767CT25GENIChomozygous109070115
2038509073850908CT12GENIChomozygous109070117
2038511603851161GA12GENIChomozygous109070119
2038513193851320CT17GENIChomozygous109070121
2038516783851679TC5GENIChomozygous109417535
2038519323851933TC10GENIChomozygous109070125
2038523833852384GA9GENIChomozygous109070127
2038529423852942TGAGG13GENIChomozygous129651561
2038529893852990AG14GENIChomozygous109070129
2038530123853013GT13GENIChomozygous109070131
2038530573853058GA13GENIChomozygous109070133
2038541063854107GA12GENIChomozygous109070135
2038544923854493AG11GENIChomozygous109070139
2038555183855519GA15GENIChomozygous109417537
2038564283856429CT16GENIChomozygous109417539
2038566613856662CT10GENIChomozygous109465719
2038567433856743CACACT12GENIChomozygous131227113
2038567573856757CT15GENIChomozygous131227114
2038585683858569C12GENIChomozygous129651563
2038567503856751TA15GENIChomozygous131235616