chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264095442264095443AG20GENICpossibly homozygous965886230
1264095886264095887AG19GENIChomozygous965886231
1264097432264097433TC25GENIChomozygous965886232
1264097633264097634AC32GENIChomozygous965886233
1264097682264097683GA29GENICpossibly homozygous965886234
1264099882264099883CT22GENIChomozygous965886235
1264099931264099932CT27GENIChomozygous965886236
1264100059264100060TA23GENICpossibly homozygous965886237
1264100188264100189AG14GENIChomozygous965886238
1264100432264100433GA37GENIChomozygous965886239
1264100637264100638TC37GENIChomozygous965886240
1264100851264100852AG23GENIChomozygous965886241
1264100853264100854AT25GENIChomozygous965886242
1264101191264101192TC12GENIChomozygous965886243
1264101725264101726TA25GENIChomozygous965886244
1264101841264101842AG15GENIChomozygous965886245
1264102013264102014GA23GENICpossibly homozygous965886246
1264102022264102023CT23GENICpossibly homozygous965886247
1264102091264102092GA24GENIChomozygous965886248
1264102112264102113TC24GENIChomozygous965886249
1264102373264102374GA18GENIChomozygous965886250
1264102418264102419TC26GENIChomozygous965886251
1264102632264102633CT25GENIChomozygous965886252
1264103104264103105GA8GENIChomozygous965886253
1264103285264103286AG16GENIChomozygous965886254
1264103682264103683CT26GENIChomozygous965886255
1264104414264104415GA20GENICpossibly homozygous965886256