chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73193453931934540AG22GENICheterozygous53863108
73193458931934590GA13GENICpossibly homozygous54643334
73193578931935790AC15GENIChomozygous53863110
73193797431937975GC26GENIChomozygous53863117
73193956031939561CT13GENIChomozygous54643336
73194056231940563GT20GENIChomozygous53863121
73194059831940599CCA17GENIChomozygous53863122
73194143531941436AT9GENICheterozygous53863123
73194280931942810A-2GENIChomozygous53863125
73194296831942970TT--10GENIChomozygous54643338
73194396531943966CT14GENIChomozygous54643340
73194487131944872TC10GENIChomozygous53863130
73194511231945113GA20GENICpossibly homozygous54643344
73194523831945239CA10GENICheterozygous53863131
73194627031946271GC16GENICpossibly homozygous53863133
73194745931947460GA17GENIChomozygous53863134
73194844631948447GA26GENICpossibly homozygous54643346
73194955531949556AG16GENIChomozygous53863137
73195056631950567TTA4GENICheterozygous53863138
73195215031952151AG25GENIChomozygous54643348
73195245831952459GA2GENICheterozygous54643350
73195375031953751TC14GENIChomozygous53863145
73195515631955157AG17GENICpossibly homozygous53863146
73195566131955662CT28GENICpossibly homozygous54643352
73195762631957627GA21GENIChomozygous54643354
73195800331958004AG14GENIChomozygous53863150
73195806731958068AC6GENICheterozygous53863151