chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
59226907592269076GT12GENIChomozygous555828819
59226961292269613CCG11GENIChomozygous704986097
59226974992269750AG13GENIChomozygous555828820
59226982092269821CT16GENIChomozygous555828821
59227056392270564GT10GENIChomozygous555828822
59227058392270588TTCTG-----8GENIChomozygous704986098
59227072392270724TC8GENIChomozygous555828823
59227105092271051AG15GENIChomozygous555828824
59227108992271090GA7GENIChomozygous555828825
59227132292271323TTA3GENIChomozygous704986099
59227250592272506CT22GENIChomozygous555828826
59227279092272791GT20GENICpossibly homozygous555828827
59227283892272839GT19GENIChomozygous555828828
59227291392272914AG15GENIChomozygous555828829
59227383292273833TC10GENIChomozygous557911086
59227418892274189CT12GENIChomozygous557911087
59227459892274599GA21GENIChomozygous557911088
59227464592274646AC20GENIChomozygous557911089
59227492292274923AG9GENIChomozygous557911090
59227506992275070GA12GENIChomozygous557911091
59227522792275228CT13GENIChomozygous557911092
59227571492275715TG19GENIChomozygous555828830
59227602792276028GA16GENIChomozygous555828831
59227660492276605CG22GENIChomozygous555828832