chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205927605205927606GA14GENIChomozygous532280629
1205928752205928753CT18GENICpossibly homozygous532280630
1205930160205930161TTAGC34GENIChomozygous693494708
1205930416205930417CT21GENICpossibly homozygous529381601
1205930522205930523CT25GENIChomozygous529381602
1205930590205930595TTTTT-----1GENIChomozygous693494709
1205930694205930695GGC2GENIChomozygous693494710
1205931569205931570AG25GENIChomozygous529381603
1205931907205931908GA19GENIChomozygous529381604
1205933575205933576TTG26GENIChomozygous693494712
1205934239205934240AC23GENIChomozygous532280631
1205934704205934705AG18GENIChomozygous532280632
1205936755205936756GA21GENIChomozygous529381605
1205937469205937470AG24GENIChomozygous529381606
1205937694205937695TC25GENIChomozygous532280633
1205937721205937722TC33GENIChomozygous529381607