chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106319746463197465AG29GENIChomozygous804063635
106319929563199296TC18GENIChomozygous804063636
106320144063201441AG36GENIChomozygous804063637
106320170563201706TG15GENIChomozygous804063638
106320210063202101CT26GENIChomozygous804063639
106320212263202123CT27GENIChomozygous804063640
106320343363203434AC16GENIChomozygous804063641
106320638863206389CA18GENIChomozygous804063642
106320740263207403TC33GENIChomozygous804063643
106320841363208414CT15GENIChomozygous804063644
106320944563209446GA19GENIChomozygous804063645
106321088363210884AG26GENIChomozygous804063646
106321177063211771CA26GENIChomozygous804063647
106321220063212201TG8GENIChomozygous804063648
106321255663212557TG27GENIChomozygous804063649
106321333663213337GA12GENIChomozygous804063650
106321347063213471AG18GENIChomozygous804063651
106321424663214247AC11GENIChomozygous804063652
106321530763215308GA29GENICpossibly homozygous804063653
106321844863218449TC15GENIChomozygous804063654
106322053363220534AC19GENIChomozygous804063655
106322265963222660CT13GENIChomozygous804063656
106322320863223209GA14GENIChomozygous804063657
106322627363226274CT9GENICpossibly homozygous804063658
106322853463228535AT22GENIChomozygous804063659
106323056563230566TC11GENIChomozygous804063660
106323109163231092GA16GENIChomozygous804063661
106323130863231309CT13GENIChomozygous804063662
106323314163233142CT24GENIChomozygous804063663