chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5143485641143485642CCA5GENICheterozygous768841363
5143485641143485642CCAAA5GENICheterozygous768841364
5143487391143487392AG17GENIChomozygous670802082
5143489159143489160AC17GENICpossibly homozygous670802083
5143489322143489323GA16GENIChomozygous670802084
5143489800143489801CT20GENIChomozygous670802085
5143491429143491430AG19GENICpossibly homozygous670802086
5143492236143492237CT25GENICheterozygous670802087
5143492550143492551GA12GENIChomozygous670802088
5143494974143494975CT21GENIChomozygous670802089
5143500737143500739TA--8GENICheterozygous768841366
5143508606143508607GA4GENICheterozygous670802090
5143512197143512198CT19GENICheterozygous670802091
5143512403143512404TC20GENICpossibly homozygous670802092
5143514376143514377AC13GENIChomozygous670802093
5143514977143514978TC17GENIChomozygous670802094
5143516152143516153GGT8GENICheterozygous768841371
5143518310143518311TC20GENICpossibly homozygous670802095
5143523066143523067CT19GENIChomozygous670802096
5143524691143524692CT10GENIChomozygous670802097
5143525318143525319GA13GENICheterozygous670802098
5143526655143526656AG22GENICpossibly homozygous670802099
5143527141143527142AC8GENICheterozygous670802100
5143527184143527185CA8GENICpossibly homozygous670802101
5143527395143527396TC13GENICpossibly homozygous670802102
5143529368143529369CT23GENIChomozygous670802103
5143531328143531329TC11GENICpossibly homozygous670802104
5143532111143532112TTTTTG5GENICheterozygous768841372