chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4165049772165049773TTA12GENIChomozygous57844234
4165049805165049806CT19GENIChomozygous58180619
4165050532165050533AATTTTTTTTT6GENICheterozygous58352935
4165051322165051323GA33GENICpossibly homozygous58180643
4165051794165051795TTG16GENICpossibly homozygous57844237
4165054886165054908GTGTGTGTGTGTGTGTGTGTGT----------------------19GENIChomozygous59651330
4165050217165050229ATTATATGCACA------------13GENICheterozygous59651326
4165052470165052471CT19GENIChomozygous59651327
4165053603165053604CCT22GENIChomozygous59651328
4165054283165054284CT24GENIChomozygous59651329
4165056767165056768CCT18GENICheterozygous58821855
4165057429165057430T-6GENIChomozygous57844243
4165059177165059178GA28GENIChomozygous59651331
4165059921165059922C-7GENIChomozygous59651332
4165059923165059926TTC---7GENIChomozygous59651333
4165060221165060225ATTT----12GENIChomozygous57844249
4165060255165060256AT9GENIChomozygous57844250
4165060256165060257GGT9GENIChomozygous57844251
4165060258165060259GA9GENIChomozygous58595961
4165060289165060290GA9GENIChomozygous57844252
4165060474165060475GA10GENIChomozygous57844253
4165060505165060506TTTTTTTTTTGG2GENIChomozygous58352943
4165060516165060517CT2GENIChomozygous58352945
4165060531165060532CT1GENIChomozygous59651334
4165060555165060556TG8GENIChomozygous58352947
4165060559165060560GC8GENIChomozygous57844254
4165060614165060615AAACACAC13GENIChomozygous59651335
4165060745165060746AG22GENIChomozygous58180720
4165061167165061168AG23GENIChomozygous57844257
4165061385165061386GA21GENIChomozygous57844258
4165062160165062161AG31GENIChomozygous57844259
4165062959165062960AT21GENIChomozygous57844261
4165063009165063010GA23GENIChomozygous57844262
4165063398165063399AG23GENIChomozygous59651336
4165063440165063441TC25GENIChomozygous57844263
4165060554165060555GGC9GENIChomozygous57546542