chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172680876626808767TC48GENIChomozygous111011112
172681339326813394GA79GENIChomozygous111011114
172681633626816337CT60GENIChomozygous111011116
172681799726817998TG29GENIChomozygous111011118
172681866726818668AT69GENIChomozygous111011120
172682413426824135GC56GENIChomozygous111011122
172682425826824259AG51GENIChomozygous111011124
172682513226825133AG64GENIChomozygous111011126
172682547326825474CT52GENIChomozygous111011128
172682547626825477CT52GENIChomozygous111011130
172682555826825559CT58GENIChomozygous111011132
172682756526827573ATACATAC39GENIChomozygous129439379
172682490426824904AC66GENIChomozygous129439376
172682669726826697TACCAACT38GENIChomozygous129439377
172682669926826699GCT42GENIChomozygous129439378
172682945326829454GA5GENIChomozygous119271361
172682984826829980GCTCCCACTGCCTGCTCACACCCAGTACACTGCGCTCCCGCTGCCTGCTCACACCCAGTACACTGTGCTCCCACTGCCTGCTCACACCCAGTACACTGTGCTCCCGCTGCCTGCTCACACCCAGTACACTGT25GENICheterozygous129439380
172683000626830007CG29GENICpossibly homozygous119271367
172683001626830017TC33GENICpossibly homozygous119271368
172683018826830188T56GENIChomozygous129439381
172683182226831823AG57GENIChomozygous111011134
172683009526830096GT58GENICpossibly homozygous111445952