chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117405787974057880AATGT7GENIChomozygous50832157
117405790674057907CT14GENICheterozygous50832158
117405791074057911AG13GENICheterozygous50832159
117405791474057915CG11GENICheterozygous50832160
117406322574063226AACTGAGCCATCTCTCCAGCCC13GENIChomozygous50832162
117406377574063776AAT12GENICpossibly homozygous50832163
117406377574063776AAC12GENICheterozygous50892691
117407849074078491AC10GENIChomozygous50832164
117408233074082331TC25GENICheterozygous50832166
117408244174082442CA8GENICheterozygous50832167
117408299774082998GT26GENICpossibly homozygous50832169
117408499174084995ATTT----22GENIChomozygous50832170
117408703774087038AATCATCTT28GENIChomozygous50832171
117408704974087050AC40GENICheterozygous50892693