chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85515560955155610T-4GENIChomozygous53207237
85515645155156452TG29GENICpossibly homozygous53207238
85515801455158015TG17GENIChomozygous53207239
85516001655160017CT14GENICpossibly homozygous52640877
85516035055160352AT--3GENIChomozygous52640879
85516433855164339CA27GENICpossibly homozygous52640881
85516438555164386GT11GENIChomozygous52640883
85516522955165232AAG---9GENIChomozygous52640885
85516669555166696AG26GENIChomozygous52640887
85516964455169645TG22GENIChomozygous52640891
85517324755173248AG13GENICpossibly homozygous52640893
85517365255173653TC17GENICheterozygous52640895
85517779055177791TA4GENIChomozygous52640897
85517779555177796CA4GENIChomozygous52640899
85517779655177797CT4GENIChomozygous52640901
85517872155178722A-4GENICheterozygous53614925
85517942055179421TC16GENIChomozygous52640907
85518035655180357GA20GENICpossibly homozygous52640917
85518043655180437GC12GENICpossibly homozygous52977928
85518103655181037AAT10GENIChomozygous53207240
85518248955182490CCT7GENIChomozygous52640931
85518347355183474GA8GENIChomozygous53207242
85518683355186834T-2GENIChomozygous52640959
85518711755187118TC12GENIChomozygous52640963
85519312355193124AG18GENIChomozygous52640967
85519333155193332CT21GENIChomozygous53207243
85519388055193881GA12GENIChomozygous52640973