chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148346055683460557AT38GENIChomozygous113604548
148346197083461972CC38GENIChomozygous131145173
148346210483462105CT52GENIChomozygous113604549
148346417983464180TC60GENIChomozygous113604550
148346548683465487CG39GENIChomozygous113604551
148346560183465601C23GENIChomozygous131145175
148346715583467156TC61GENIChomozygous113604552
148346751883467521ACG57GENIChomozygous131145176
148346822383468224A55GENICpossibly homozygous131145177
148347060383470603CA43GENICpossibly homozygous131145178
148347271883472719GC49GENIChomozygous113604553
148347371583473716GA47GENIChomozygous113604554
148347430583474306AT50GENIChomozygous113679897
148347445783474458AC54GENIChomozygous131151552
148347458783474588TC57GENIChomozygous113679899
148347460683474607GA53GENIChomozygous113604555
148347469383474694GA39GENIChomozygous113604556
148347595883475959TC38GENIChomozygous118765771