chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121057514210575143TG18GENIChomozygous953175755
121057647310576474TA32GENIChomozygous953175756
121057647710576478TG32GENIChomozygous953175757
121057726310577264GT30GENIChomozygous953175758
121057776610577767GT30GENIChomozygous953175759
121057816510578166AG20GENIChomozygous953175760
121058054410580545TC12GENIChomozygous953175761
121058068210580683TC22GENIChomozygous953175762
121058277210582773CT24GENIChomozygous953175763