chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
397928299792830AG11GENIChomozygous111443612
397928439792844G11GENIChomozygous132038440
397932079793208TC11GENIChomozygous111443613
397932479793248CT18GENIChomozygous111443614
397933039793304TG19GENIChomozygous111443615
397942289794229TG24GENIChomozygous111443616
397942629794263GA19GENIChomozygous111443617
397944439794444AG16GENIChomozygous111443618
397944609794461CT12GENIChomozygous111443619
397947469794747TC26GENIChomozygous111443620
397947569794757TC27GENIChomozygous111443621
397949039794904TC14GENIChomozygous111443622
397950649795065CT27GENIChomozygous111443623
397953779795378TC13GENIChomozygous111443625
397954799795480CT18GENIChomozygous111443627
397954899795490CG19GENIChomozygous111443628
397962729796273TC18GENIChomozygous111443630
397962969796297AT19GENIChomozygous111443631
397963839796384GA17GENIChomozygous111443632
397965629796563TG14GENIChomozygous111443633
397966089796609AG16GENIChomozygous111443634
397969129796913GT30GENICpossibly homozygous111443635
397970879797088TC13GENIChomozygous111443636
397972039797204GA24GENIChomozygous111443637
397973399797340CT18GENIChomozygous111443638
397974879797488AG19GENIChomozygous111443639
397955699795570CT21GENIChomozygous112065537
397975569797559ATC20GENIChomozygous127848649
397935919793592C11GENIChomozygous127848647
397967649796764C17GENIChomozygous127848648
397981469798147CT25GENIChomozygous111443640
397983489798349AC18GENIChomozygous111443641
397985969798597GA21GENIChomozygous112065539
397986339798634CG21GENIChomozygous111443642
397987149798715AG23GENIChomozygous111443643
397987779798778CT19GENIChomozygous111443644