chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005837210058373AG27GENIChomozygous967831539
141005839310058394AC28GENICpossibly homozygous967831540
141005854510058546CA27GENIChomozygous967831541
141005858910058590CT32GENIChomozygous967831542
141005869510058696CT38GENIChomozygous967831543
141005889610058897GA37GENIChomozygous967831544
141005934910059350GA21GENIChomozygous967831545
141006074310060744CT18GENIChomozygous967831546
141006082010060821AG13GENIChomozygous967831547
141006096610060967CT22GENIChomozygous967831548
141006108710061088GC25GENIChomozygous967831549
141006114010061141CT20GENIChomozygous967831550
141006114210061143AT20GENIChomozygous967831551
141006115310061154TC19GENIChomozygous967831552
141006119810061199GA24GENIChomozygous967831553
141006141410061415AC29GENIChomozygous967831554
141006142010061421GA30GENIChomozygous967831555
141006142310061424TA28GENIChomozygous967831556
141006144610061447CA31GENIChomozygous967831557
141006159510061596GA29GENIChomozygous967831558
141006163110061632CT26GENIChomozygous967831559
141006168610061687TC29GENIChomozygous967831560
141006169310061694AG33GENIChomozygous967831561
141006169410061695AG33GENIChomozygous967831562
141006170010061701CT32GENIChomozygous967831563
141006187310061874GA18GENIChomozygous967831564
141006187510061876CA18GENIChomozygous967831565