chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264538051264538052GT16GENIChomozygous108783308
1264538198264538199CT18GENIChomozygous109027604
1264538804264538805CT29GENIChomozygous108783309
1264540468264540469CT22GENICpossibly homozygous108783311
1264540973264540974CT23GENICpossibly homozygous108783313
1264541122264541123CT25GENIChomozygous108783314
1264542002264542003CT15GENIChomozygous108783315
1264542350264542351TC27GENIChomozygous108783317
1264542657264542658AC23GENIChomozygous108783318
1264542680264542681TC17GENIChomozygous108783319
1264542841264542842TC27GENIChomozygous108783320
1264543227264543228CT35GENIChomozygous108783321
1264543788264543789AC23GENIChomozygous109027605
1264551912264551913TC25GENICheterozygous108636296
1264551930264551931TC23GENICheterozygous108636297
1264551936264551937GC23GENICheterozygous108636298
1264558419264558420TC27GENIChomozygous108636311
1264558504264558505AG27GENIChomozygous109027606
1264559413264559414GC23GENIChomozygous108783334
1264559594264559595CG37GENIChomozygous109027607
1264559925264559926GA22GENIChomozygous109027608
1264560268264560269TC19GENIChomozygous108636318
1264560454264560455TC20GENIChomozygous108636319
1264561369264561370GA31GENIChomozygous108636322
1264561479264561480GA27GENIChomozygous108783335
1264562786264562787TC24GENIChomozygous108636327
1264563304264563305AG19GENIChomozygous109027609
1264563727264563728AG24GENIChomozygous108636328