chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175402931254029313TG23GENIChomozygous111247743
175402931454029314G23GENIChomozygous131192597
175403563654035637GA14GENIChomozygous111247745
175403569754035781ACGCCTGCCCGGGATGTGACATTAGGCATCCTCTTACATGGGCACTTCTCTGCAGTGCAGTCTCTCATGTTGGTGAACAACAGA14GENIChomozygous131192598
175404010354040104AG13GENIChomozygous111063824
175404041354040414TC19GENIChomozygous111247747
175404049654040497G14GENIChomozygous131192599
175404082054040822GA10GENIChomozygous131192600
175404088354040884AT8GENIChomozygous111063826
175404366154043662C20GENIChomozygous131192601
175404394554043946CA8GENIChomozygous111247749
175404592954045930TA9GENIChomozygous111063834
175404674154046742CT12GENIChomozygous111247751
175404790054047900C2GENIChomozygous131192602
175404895654048957GA13GENIChomozygous111063837
175404920154049202TG10GENIChomozygous111247753
175405041254050413AG19GENIChomozygous111063839
175405081554050816CT9GENIChomozygous111247755
175405210354052104CA20GENIChomozygous111247757
175405323554053236CA21GENIChomozygous111063842
175405739454057395CA16GENIChomozygous111063849
175405795254057953TC24GENIChomozygous111063850
175405639854056399GA7GENIChomozygous111426986
175405536954055370CT17GENIChomozygous119391434
175405538654055387AT16GENIChomozygous119391436
175405577154055772GA10GENIChomozygous119391438
175405860354058604AC8GENIChomozygous119293590
175405897954058980AG26GENIChomozygous111247759
175406175254061753GA20GENIChomozygous119391439
175406284954062850GA21GENIChomozygous111205142
175406532254065322T13GENIChomozygous129458479
175406784754067848TC23GENIChomozygous111063856
175406999154069992GA18GENIChomozygous111247761
175407019254070193GT28GENIChomozygous111063859