chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102769327527693276AAGTCTCT1GENIChomozygous51380107
102769336827693369AG5GENICheterozygous51380115
102769382727693828CCT9GENICheterozygous51380117
102769483127694832CCT4GENICheterozygous51380119
102769502527695029ATTA----2GENIChomozygous51380121
102769868827698689AAAC2GENIChomozygous51380125
102769869327698694AC2GENIChomozygous51380127
102769890027698901AG18GENIChomozygous51380129
102769920327699204GA9GENICpossibly homozygous51380131
102770121527701216GT11GENIChomozygous51380133
102770247627702477T-1GENIChomozygous51380137
102770310127703103TA--8GENIChomozygous51380139
102770333427703335TC20GENIChomozygous51380141
102770338427703385AATC6GENIChomozygous51380143
102770339327703394CT6GENIChomozygous51380145
102770350327703504CT22GENIChomozygous51380147
102770353527703536CT12GENICpossibly homozygous51380149
102770379027703791TC15GENICheterozygous51380151
102770411427704115TC5GENIChomozygous51380153
102770422227704223AC17GENIChomozygous51380157
102770424627704247AC9GENICpossibly homozygous51380159
102770446427704465CT6GENICheterozygous51380161
102770456427704565GA9GENICpossibly homozygous51380163
102770460227704603AT7GENICpossibly homozygous51380165
102770490727704910AAA---3GENIChomozygous51380167
102770503227705033TC11GENIChomozygous51380169
102770508727705088AC23GENICpossibly homozygous51380171
102770556927705570GA21GENIChomozygous51380173
102770560127705602AACTT5GENICheterozygous51380175
102770596427705965AC14GENICpossibly homozygous51380177
102770621827706219AG6GENIChomozygous51380178
102770622827706229TC2GENIChomozygous51380180
102770624427706245TC7GENIChomozygous51380182
102770694827706949AG29GENICpossibly homozygous51380188
102770247827702479TG1GENIChomozygous52315180
102770623727706238CCCACACACACACACACACACACA3GENIChomozygous52315181
102770653127706532A-3GENIChomozygous52315182