chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106319746463197465AG21GENIChomozygous786334660
106319929563199296TC27GENIChomozygous786334661
106320144063201441AG14GENIChomozygous786334662
106320170563201706TG26GENIChomozygous786334663
106320210063202101CT27GENIChomozygous786334664
106320212263202123CT25GENIChomozygous786334665
106320343363203434AC17GENIChomozygous786334666
106320638863206389CA32GENIChomozygous786334667
106320740263207403TC21GENIChomozygous786334668
106320841363208414CT23GENIChomozygous786334669
106320944563209446GA25GENIChomozygous786334670
106321088363210884AG23GENIChomozygous786334671
106321177063211771CA13GENIChomozygous786334672
106321220063212201TG4GENIChomozygous786334673
106321221263212213TG5GENIChomozygous786334674
106321255663212557TG24GENIChomozygous786334675
106321333663213337GA14GENIChomozygous786334676
106321347063213471AG24GENIChomozygous786334677
106321424663214247AC16GENIChomozygous786334678
106321530763215308GA21GENIChomozygous786334679
106321844863218449TC27GENIChomozygous786334680
106322053363220534AC30GENIChomozygous786334681
106322265963222660CT28GENIChomozygous786334682
106322320863223209GA26GENIChomozygous786334683
106322627363226274CT30GENIChomozygous786334684
106322853463228535AT33GENIChomozygous786334685
106323056563230566TC29GENICpossibly homozygous786334686
106323109163231092GA22GENIChomozygous786334687
106323130863231309CT22GENIChomozygous786334688
106323314163233142CT24GENIChomozygous786334689