chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5142732231142732232AG24GENIChomozygous114253209
5142733099142733100AG18GENIChomozygous114253211
5142733264142733265TC17GENIChomozygous114033936
5142733491142733492GT6GENIChomozygous114033937
5142733568142733569C2GENIChomozygous131651115
5142734139142734140GA11GENIChomozygous114253213
5142734435142734436TG4GENIChomozygous114033942
5142734450142734451TC5GENIChomozygous114253215
5142735383142735384TC15GENIChomozygous114033945
5142737460142737460A18GENIChomozygous131651116
5142739269142739270A18GENICpossibly homozygous131651117
5142739500142739501CT15GENIChomozygous114253227
5142740618142740618T14GENIChomozygous131651118
5142741099142741100TC16GENIChomozygous114033951
5142742062142742063GA14GENIChomozygous114033953
5142742487142742488AG22GENIChomozygous114033955
5142743841142743841T7GENIChomozygous131651119
5142763516142763517GA4GENIChomozygous126205380
5142763848142763849TC3GENICheterozygous114033959
5142763806142763808TC5GENICheterozygous128248648
5142743632142743633TG1GENIChomozygous114445681