chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4150927701150927702CT34GENIChomozygous58158251
4150927960150927961GA17GENIChomozygous58158253
4150927963150927964AG18GENIChomozygous58158255
4150928639150928640GA20GENIChomozygous58158257
4150928969150928970AG26GENIChomozygous58158259
4150930404150930405TC19GENIChomozygous58158261
4150930676150930677AT11GENIChomozygous58286320
4150930677150930678TTTA11GENIChomozygous58158263
4150931237150931238GA34GENIChomozygous58158265
4150932489150932490AG18GENIChomozygous56982220
4150933289150933295TGTGTG------7GENIChomozygous58346320
4150933518150933526CTCTCTCT--------3GENICheterozygous58407696
4150935108150935109TC19GENIChomozygous58158267
4150936222150936223AAAGCAGAGCAGAGCAGAGCAGAGCAGAGCAG4GENIChomozygous58346322
4150936595150936596CT20GENIChomozygous58158271
4150938183150938184TC19GENIChomozygous58158273
4150938454150938455CA25GENIChomozygous58158275
4150938909150938910TTTC16GENICpossibly homozygous58346324
4150938956150938966ACACACACAC----------8GENIChomozygous58346326
4150939797150939798GA34GENICpossibly homozygous58158277
4150940406150940407AG37GENIChomozygous58158279
4150941548150941549CA18GENIChomozygous58158281
4150942178150942182AGGG----9GENIChomozygous58346328
4150942229150942230AG14GENIChomozygous58158283
4150942287150942291AAAG----9GENIChomozygous58346330
4150942428150942432AAAG----11GENIChomozygous58158285
4150942514150942515GT20GENIChomozygous58158289
4150942597150942605AGGAAGGA--------6GENIChomozygous57518714
4150944320150944321TTG8GENIChomozygous57518716
4150944430150944431GA24GENIChomozygous58158293
4150944479150944480GA27GENIChomozygous58158295
4150944614150944615GA25GENIChomozygous58158297