chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1169927205169927206GA17GENICpossibly homozygous783687479
1169927351169927352CA33GENIChomozygous783687480
1169927403169927404CT33GENIChomozygous783687481
1169927472169927473TC34GENIChomozygous783687482
1169927498169927499CT29GENIChomozygous783687483
1169927525169927526CA28GENIChomozygous783687484
1169927623169927624AT23GENIChomozygous783687485
1169927625169927626CA23GENIChomozygous783687486
1169927631169927632TG23GENIChomozygous783687487
1169927638169927639TA26GENIChomozygous783687488
1169927695169927696AC23GENIChomozygous783687489
1169927718169927719AG21GENIChomozygous783687490
1169927719169927720CT21GENIChomozygous783687491
1169927771169927772GA22GENIChomozygous783687492
1169927888169927889TC29GENIChomozygous783687493
1169928004169928005AT24GENIChomozygous783687494