chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1143041437143041438A-12GENICheterozygous60877219
1143042539143042542TCT---3GENIChomozygous62089380
1143043070143043073TTT---7GENICheterozygous60877224
1143043072143043073T-7GENICheterozygous60877225
1143044194143044195CT20GENIChomozygous60877226
1143044197143044198TA19GENIChomozygous60877227
1143045125143045126T-31GENICpossibly homozygous60877228
1143048041143048042AG22GENIChomozygous60877229
1143050618143050619GT22GENIChomozygous60877231
1143050771143050777GTGTGT------14GENICpossibly homozygous60877233
1143053170143053171TG20GENIChomozygous60877239
1143053812143053813CA14GENIChomozygous60877241
1143053818143053819A-16GENIChomozygous60877242
1143057030143057031TC19GENIChomozygous60877243