chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117817276378172764AG19GENIChomozygous50834989
117817284178172845AAAC----8GENIChomozygous50834990
117818272778182729AC--7GENIChomozygous50834993
117818311578183116CT11GENIChomozygous50834994
117818322578183226GGC8GENIChomozygous50834995
117818773378187734CT15GENIChomozygous50834999
117818804078188041TC25GENIChomozygous50835000
117818841178188412TC8GENIChomozygous50835002
117818857078188571CT3GENIChomozygous50835003
117818861878188619GGC6GENIChomozygous50835004
117818906078189061GA14GENIChomozygous50835005
117818910078189101AAT4GENIChomozygous50835006
117818911678189117CT9GENICpossibly homozygous50835007
117818923578189236CT21GENIChomozygous50835008
117818932178189322AG21GENICpossibly homozygous50835009