chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1216257450216257451AG18GENIChomozygous108535669
1216258379216258380TC17GENIChomozygous109193138
1216258516216258517TC19GENIChomozygous108535671
1216262145216262146TG18GENIChomozygous108535673
1216262321216262322CT17GENIChomozygous108535674
1216262484216262485AG16GENIChomozygous108535675
1216263375216263376CT14GENIChomozygous125438481
1216264012216264013TC11GENIChomozygous108535676
1216264464216264465GA33GENIChomozygous125438482
1216264534216264535AC24GENIChomozygous108535677
1216264583216264584AG13GENIChomozygous108535678
1216265607216265608AG28GENIChomozygous108535681
1216266590216266591CT25GENIChomozygous108535683
1216268775216268776GC10GENIChomozygous108535684
1216269220216269221TC14GENIChomozygous108535685
1216270191216270192TG18GENIChomozygous108535687
1216270300216270301AG20GENIChomozygous108535688
1216271519216271520CT27GENIChomozygous125438484
1216272100216272101TC14GENIChomozygous125438485
1216272466216272467GA8GENIChomozygous125438487
1216273927216273928CT14GENIChomozygous125438489
1216274441216274442GC21GENIChomozygous125438490
1216274462216274463AG23GENIChomozygous108535690
1216274763216274764CT23GENIChomozygous125438492
1216275449216275450AG20GENIChomozygous120843981
1216275563216275564AG15GENIChomozygous108535692
1216276291216276292TG15GENIChomozygous125438493
1216276523216276524TC28GENIChomozygous125438494
1216277048216277049TC13GENIChomozygous108535693
1216277523216277524TG16GENIChomozygous125438495
1216277821216277822TG25GENIChomozygous125438496
1216277861216277862CA15GENIChomozygous125438497
1216265037216265038AG17GENIChomozygous125535114
1216269787216269788AG17GENIChomozygous125535115
1216270210216270211GA9GENIChomozygous125535116
1216271658216271659GA13GENIChomozygous125535117
1216279511216279512CT16GENIChomozygous125438498
1216279715216279716GA19GENIChomozygous125438499
1216280027216280028TC12GENIChomozygous120843985