chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135008154135008155CT35GENIChomozygous114144245
5135008781135008782GT44GENICheterozygous114144246
5135011563135011564CG49GENICpossibly homozygous114144247
5135011990135011991AG47GENIChomozygous114144248
5135012555135012556CT45GENIChomozygous114144249
5135012559135012560CT46GENIChomozygous114144250
5135014215135014216GT54GENIChomozygous114017528
5135014663135014664GA27GENICpossibly homozygous114144251
5135014968135014969CT43GENIChomozygous114144252
5135015384135015385AT52GENIChomozygous114144253
5135015414135015415GA59GENIChomozygous114144254
5135015719135015720GA43GENIChomozygous114144255
5135016052135016053GA47GENIChomozygous114017536
5135016310135016311TC47GENIChomozygous114017537
5135017089135017090AG42GENIChomozygous114017538