chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121057443110574432GA15GENIChomozygous781747860
121057701610577017TG54GENICpossibly homozygous781747861
121057726310577264GT43GENIChomozygous781747862
121057776610577767GT74GENIChomozygous781747863
121057816510578166AG58GENIChomozygous781747864
121057956110579562GA83GENICpossibly homozygous781747865
121058054410580545TC47GENIChomozygous781747866
121058068210580683TC57GENIChomozygous781747867
121058277210582773CT54GENIChomozygous781747868
121058298310582984AG45GENICpossibly homozygous781747869