chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3161272905161272912TTGTTTT18GENIChomozygous127949000
3161274735161274736AG23GENIChomozygous111797022
3161276873161276874GA19GENIChomozygous111797024
3161277028161277029AC22GENICpossibly homozygous111797026
3161279343161279347CTGT24GENIChomozygous127949001
3161279872161279873T19GENIChomozygous127949002
3161280750161280751AC29GENIChomozygous111797027