chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1143041437143041438A-10GENICpossibly homozygous60877219
1143043072143043073T-6GENIChomozygous60877225
1143044194143044195CT15GENIChomozygous60877226
1143044197143044198TA15GENIChomozygous60877227
1143045125143045126T-16GENIChomozygous60877228
1143048041143048042AG22GENIChomozygous60877229
1143050618143050619GT26GENIChomozygous60877231
1143050771143050777GTGTGT------8GENIChomozygous60877233
1143053170143053171TG15GENIChomozygous60877239
1143053812143053813CA11GENIChomozygous60877241
1143053818143053819A-13GENIChomozygous60877242
1143057030143057031TC13GENIChomozygous60877243
1143042539143042542TCT---15GENIChomozygous62089380