chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005837210058373AG31GENIChomozygous948046316
141005839310058394AC30GENIChomozygous948046317
141005854510058546CA26GENIChomozygous948046318
141005889610058897GA28GENIChomozygous948046319
141006082010060821AG11GENIChomozygous948046320
141006091510060916TA16GENIChomozygous948046321
141006096610060967CT15GENIChomozygous948046322
141006108710061088GC22GENIChomozygous948046323
141006114010061141CT23GENIChomozygous948046324
141006115310061154TC24GENIChomozygous948046325
141006119810061199GA37GENIChomozygous948046326
141006141410061415AC29GENIChomozygous948046327
141006142010061421GA28GENIChomozygous948046328
141006142310061424TA28GENIChomozygous948046329
141006144610061447CA24GENIChomozygous948046330
141006157910061580AG38GENIChomozygous948046331
141006158510061586AG35GENIChomozygous948046332
141006159510061596GA34GENIChomozygous948046333
141006163110061632CT28GENIChomozygous948046334
141006168610061687TC39GENIChomozygous948046335
141006169310061694AG37GENIChomozygous948046336
141006169410061695AG38GENIChomozygous948046337
141006170010061701CT39GENIChomozygous948046338
141006187310061874GA26GENIChomozygous948046339
141006187510061876CA27GENIChomozygous948046340