chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8108596292108596293GA8GENIChomozygous138411601
8108598125108598126AG18GENIChomozygous138411602
8108598133108598134AC19GENIChomozygous138411603
8108598596108598597TA15GENIChomozygous142099598
8108600549108600550AG17GENIChomozygous138411604
8108600648108600651TCT10GENICpossibly homozygous138263693
8108600845108600846TC13GENIChomozygous142099599
8108600905108600906GA7GENIChomozygous142099600
8108601814108601815GT14GENIChomozygous138411605
8108601930108601931TC7GENIChomozygous142099601
8108601956108601957AG10GENIChomozygous142099602
8108601958108601959AG10GENIChomozygous142099603
8108602388108602389CG7GENIChomozygous142099604
8108603280108603281TG13GENIChomozygous142099605
8108604653108604654TC14GENIChomozygous142099606
8108604656108604657GA14GENIChomozygous142099607
8108607907108607908TC16GENIChomozygous142099608
8108610210108610211AG21GENIChomozygous138411607
8108610278108610279CT17GENIChomozygous142099609
8108610474108610475CT23GENIChomozygous142099610