chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
119122508191225082GA20GENIChomozygous50865272
119122512791225128CT25GENIChomozygous50865273
119122525691225257CT28GENIChomozygous50865274
119122805091228051AG35GENIChomozygous50865275
119123377291233773TC31GENIChomozygous50865277
119123404791234048T-17GENIChomozygous50865278
119123443991234440AAC15GENICpossibly homozygous50865279
119123444091234441AAC12GENIChomozygous50865282
119123571791235718AG34GENIChomozygous50865283
119123732191237322CA14GENIChomozygous50865284
119123791991237920AG23GENIChomozygous50865285
119123822291238223CCAAA5GENICheterozygous50865286
119123822291238223CCAA5GENICheterozygous50898820
119123845891238459AG10GENIChomozygous50865287