chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7104500582104500583GA8GENIChomozygous115798536
7104502630104502631AG17GENIChomozygous115798538
7104502849104502850AC18GENIChomozygous118257924
7104502850104502851CA19GENIChomozygous118257926
7104503621104503622AG17GENIChomozygous115798542
7104505923104505924CA29GENIChomozygous115798544
7104506018104506019GT28GENICpossibly homozygous115798546
7104506383104506384TC22GENIChomozygous115798548
7104506692104506693AT27GENIChomozygous115798550
7104507078104507079TC30GENIChomozygous115798552
7104507088104507089GA33GENIChomozygous115798554
7104507976104507977GA19GENIChomozygous115798556
7104508348104508349AG30GENIChomozygous115798558
7104508795104508796GA17GENIChomozygous115798560
7104510607104510608AG27GENIChomozygous115798562