chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
131457969914579700AG32GENIChomozygous800050656
131457971014579711CA32GENIChomozygous800050657
131457984014579841GA24GENIChomozygous800050658
131457990114579902TA22GENIChomozygous800050659
131457995414579955AG25GENIChomozygous800050660
131457997514579976CA22GENIChomozygous800050661
131458001314580014CT29GENIChomozygous800050662
131458004714580048GA18GENIChomozygous800050663
131458044414580445CA39GENIChomozygous800050664
131458051514580516TC36GENIChomozygous800050665
131458060514580606GT34GENIChomozygous800050666
131458084314580844TC9GENIChomozygous800050667
131458084414580845GA9GENIChomozygous800050668
131458102714581028GA21GENIChomozygous800050669
131458102914581030TC21GENIChomozygous800050670
131458106114581062GA19GENIChomozygous800050671
131458121914581220AG44GENICpossibly homozygous800050672