chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
119122508191225082GA18GENIChomozygous50865272
119122512791225128CT19GENIChomozygous50865273
119122525691225257CT26GENIChomozygous50865274
119122805091228051AG15GENIChomozygous50865275
119123377291233773TC22GENIChomozygous50865277
119123404791234048T-22GENICpossibly homozygous50865278
119123443991234440AAC11GENICheterozygous50865279
119123444091234441AAC11GENIChomozygous50865282
119123571791235718AG14GENIChomozygous50865283
119123732191237322CA17GENIChomozygous50865284
119123791991237920AG30GENIChomozygous50865285
119123822291238223CCAAA12GENICheterozygous50865286
119123822291238223CCAA12GENICpossibly homozygous50898820
119123845891238459AG2GENIChomozygous50865287