chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
89703942697039427AG15GENIChomozygous138387334
89703960297039603AG16GENIChomozygous138387335
89704015197040153AT29GENIChomozygous138257847
89704032197040321T17GENIChomozygous138257848
89704034197040342TC16GENIChomozygous138387336
89704035597040356AG16GENIChomozygous138387337
89704038097040380A10GENIChomozygous138257849
89704241397042414GA16GENIChomozygous138387338
89704371797043717T11GENIChomozygous138257850
89704391697043917CT15GENIChomozygous138387339
89704392897043929TC13GENIChomozygous138387340
89704416597044166TG14GENIChomozygous138387341
89704416697044167TC14GENIChomozygous138387342
89704472797044728AT17GENIChomozygous138387343
89704492197044922GA25GENIChomozygous138387344
89704509097045091TC10GENIChomozygous138387345
89704529597045296CT19GENIChomozygous138387346
89704578997045792TTC15GENIChomozygous138257851
89704595197045951TCA24GENIChomozygous138257852
89704625297046253CT21GENIChomozygous138387347
89704653797046538CT20GENIChomozygous138387348
89704656997046570CT16GENIChomozygous138387349
89704660197046602TC14GENIChomozygous138387350
89704693097046931A16GENIChomozygous138257853
89704699697046997AG12GENIChomozygous138387351
89704783397047834TG14GENIChomozygous138387352
89704790697047907CA12GENIChomozygous138387353
89704799697047997AC20GENIChomozygous138387354